Find Compliance, Regulatory & Consulting Services for Drug Development

United Kingdom

Virtual Booth

Quotient Sciences' team possesses an in-depth understanding of the evolving clinical trial regulatory environment in Europe & the US, ensuring the production of high-quality dossiers, submission & approval process for Phase I clinical trial applications.

REGULATORY SUBMISSIONS FOR CLINICAL TRIALS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Renejix: CDMO with expertise in small molecule oral dosage, delivery tech, and multi-modality manufacturing.

Sub Category: Regulatory Affairs

Regulatory Submissions for Clinical Trials

CPhI North America

Booth #1420

envelop Contact Supplier

Renejix

Renejix offers customized regulatory affairs services for global markets and supports the full product lifecycle. Its regulatory specialists are experienced in handling a wide range of products including small molecules, NCEs & established dosage forms.

U.S.A

Virtual Booth

Digital Content

REGULATORY SUPPORT

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Quotient Sciences- Molecule to Cure. Fast.

Sub Category: Regulatory Affairs

Cophex 2024

Not Confirmed

Contact Supplier

Quotient Sciences

United Kingdom

Virtual Booth

Quotient Sciences offers modeling & simulations for formulations and clinical designs. Its experts use GastroPlus™ to model biopharmaceutical & PK data, providing valuable insights into the in-vivo performance of molecules & formulations.

CLINICAL TRIAL DESIGN

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Renejix: CDMO with expertise in small molecule oral dosage, delivery tech, and multi-modality manufacturing.

Sub Category: Clinical Trial Design

CPhI North America

Booth #1420

envelop Contact Supplier

Renejix

Renejix provides comprehensive consulting and regulatory services in cutting-edge facilities specializing in oral dosage pharmaceuticals. It offers comprehensive consultative services for cold chain requirements and controlled substance management.

U.S.A

Virtual Booth

Digital Content

CONSULTING SERVICES FOR ORAL DOSAGE FORMS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Renejix: CDMO with expertise in small molecule oral dosage, delivery tech, and multi-modality manufacturing.

Sub Category: Consulting Services

Consulting Services for Oral Dosage Forms

Cophex 2024

Not Confirmed

Contact Supplier

Renejix

Renejix regulatory specialists provide guidance and solutions to minimize product development time & accelerate product approvals. Its quality processes include quality assurance, quality systems & quality control in compliance with regulatory standards.

U.S.A

Virtual Booth

Digital Content

QUALITY & COMPLIANCE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Renejix: CDMO with expertise in small molecule oral dosage, delivery tech, and multi-modality manufacturing.

Sub Category: Quality & Compliance

Cophex 2024

Not Confirmed

Contact Supplier

Renejix

Renejix is a CDMO that provides full services for clinical trial supply packaging, labeling, storage, and delivery, assuring regulatory compliance and effective supply chain management.

U.S.A

Virtual Booth

Digital Content

REGULATORY COMPLIANCE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Overview

Cophex 2024

Not Confirmed

Contact Supplier

Lovelace Scientific Resources

U.S.A

Virtual Booth

We always ensure we are in line with the latest regulations and compliance guidelines. We thoroughly assess participant safety and ensure that the participants are committed and motivated to complete their study.

REGULATORY AFFAIRS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

KAI Research

U.S.A

Virtual Booth

We support clinical sites by confirming regulatory compliance and assisting them in preparing, editing, formatting, submitting, and tracking regulatory documents such as informed consent/assent forms, HIPAA notifications, and participant information sheets.

REGULATORY SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Icon Plc

Ireland

Virtual Booth

Our regulatory consulting team serves clients around the globe from biotech startups to big pharma as well as the research, investment, and legal firms that serve them.

STRATEGIC REGULATORY SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

PPD

U.S.A

Virtual Booth

PPD provides effective global regulatory affairs services for all stages of pharmaceutical, biologic and medical device product development and lifecycle management.

GLOBAL REGULATORY AFFAIRS SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Quorum Review, Inc.

U.S.A

Virtual Booth

Quorum understands the complexities of device research. Our boards have extensive experience with devices, our regulatory team can help determine the appropriate classifications for your product, and our support staff can guide you through the particulars of reviewing device research.

DEVICE STUDIES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Medical Devices

ASK
US

Upload
your Marketing & Sales content

PAREXEL International Corporation

U.S.A

Virtual Booth

Our Regulatory Outsourcing Services include both pre-approval and post-approval activities ranging from the compilation, publishing, and dispatching of large regulatory dossiers to the authoring of routine product variations, annual reports and other product lifecycle maintenance tasks.

REGULATORY OUTSOURCING SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

TFS International AB

Sweden

Virtual Booth

The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

PRODUCT DEVELOPMENT CONSULTING

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

DZS Clinical Services

DZS Clinical Services provides expert consultation and advice on the strategic direction of your clinical trial for your drug product or device across many therapeutic areas in the biopharmaceutical, medical device and government and nonprofit sectors.

U.S.A

Virtual Booth

Digital Content

CLINICAL DEVELOPMENT STRATEGY

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Clinical Trial Design

ASK
US

Upload
your Marketing & Sales content

Elligo Health Research

U.S.A

Virtual Booth

Our team Goes Direct with an approach that redefines the clinical trial process — finding and identifying patients for studies, then providing their physicians with the personnel, processes, technology and infrastructure to conduct them in their own clinics.

GOES DIRECT APPROACH

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Clinical Trial Design

ASK
US

Upload
your Marketing & Sales content

Litera Microsystems

DocXtool for Life Sciences is a Microsoft Word toolbar that accelerates the creation, review, and formatting of your electronic common technical document (eCTD), helping get your documents submission-ready faster.

U.S.A

Virtual Booth

Digital Content

DOCXTOOLS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Quorum Review, Inc.

U.S.A

Virtual Booth

Quorum has extensive experience with combination products. Our boards and regulatory teams understand the intricacies of combination product research. We can help determine the correct way to manage your study, and we will apply the proper standards for your product.

COMBINATION PRODUCT STUDIES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Medical Devices

ASK
US

Upload
your Marketing & Sales content

Evidera

U.S.A

Virtual Booth

Pragmatic studies aim to quantify the risks, benefits and costs of an intervention in routine clinical practice, often helping to inform how a treatment may be applied by clinicians outside of the clinical trial environment.

PRAGMATIC / ADAPTIVE STUDIES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Lovelace Scientific Resources

U.S.A

Virtual Booth

When contracting with LSR Trials, you can be assured that we will meet all deadlines and the data will be immaculate to ensure a successful trial.

QUALITY ASSURANCE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

Covigilant LLC

Covigilant’s experts provide strategic advice and risk management services in a broad range of areas for your safety-systems-related operations.

U.S.A

Virtual Booth

Digital Content

DRUG SAFETY SOLUTIONS CONSULTATION

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

TFS International AB

Sweden

Virtual Booth

The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

PROTOCOL DESIGN

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Clinical Trial Design

ASK
US

Upload
your Marketing & Sales content

MPI Research Inc

MPI Research is a full early-stage drug development CRO that partners with biopharmaceutical, biotechnology, medical device, animal health, and chemical industries to advance global healthcare. MPI Research supports all phases of the drug development pathway, ranging from target identification

U.S.A

Virtual Booth

Digital Content

SUPPORTING ALL PHASES OF DRUG DEVELOPMENT

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Factory CRO

We are well acquainted with CE-marking studies and can assure that your study can be designed and controlled to meet the demands of Notified Bodies.

U.S.A

Virtual Booth

Digital Content

CE MARKING

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

Reliance Clinical Testing Services, Inc

RCTS designs protocols in adherence with International Conference of Harmonization (ICH) and good clinical practice (GCP) guidelines, The research protocol describes in detail how the clinical trial will be conducted.

U.S.A

Virtual Booth

Digital Content

PROTOCOL DESIGN

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Overview

ASK
US

Upload
your Marketing & Sales content

Evidera

U.S.A

Virtual Booth

Our expert teams of industry leaders, former payers, policy experts, and experienced strategists can help you navigate complex evidence requirements and anticipate and overcome payer barriers to help you achieve optimal price and access.

MARKET ACCESS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Icon Plc

Ireland

Virtual Booth

Mapi provides customers with assistance on quality and compliance matters, including pharmaceutical quality assurance, medical device quality systems, and clinical compliance (GCP).

QUALITY & REGULATORY SUPPORT

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

Greenleaf Health Inc

U.S.A

Virtual Booth

Greenleaf’s advisory services include research and analysis of the following potential sources of risk: Marketing authorization; Manufacturing and quality; Promotion; Distribution and supply chain; Pipeline analysis; Compliance status; Labeling; Product safety

ADVISORY SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

TFS International AB

Sweden

Virtual Booth

The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

REGULATORY AFFAIRS STRATEGY

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

CLINICAL SUPPLIES MANAGEMENT HOLDINGS, INC.

No matter how complex your clinical supplies problems are, our experienced consulting team has the expertise and background to ensure a smooth supply process.

U.S.A

Virtual Booth

Digital Content

CLINICAL SUPPLIES & CONSULTING

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Evidera

U.S.A

Virtual Booth

Evidera’s expert team of scientists, modelers and statisticians has developed hundreds of simulations, statistical models, and literature reviews to support reimbursement, market access, and internal decision making in all major therapeutic indications and across all major markets.

MODELING & META RESEARCH

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

TFS International AB

Sweden

Virtual Booth

The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

PREPARATION & SUBMISSION OF CTA/ITA, IND, PMA / 510 (K)

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

LabConnect

U.S.A

Virtual Booth

If investigator training meetings are required, LabConnect will send a PM to your investigator training meetings in the regions you designate. A detailed laboratory manual will be developed based on the protocol and may be translated upon your request.

INVESTIGATOR TRAINING & SUPPORT

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Training

ASK
US

Upload
your Marketing & Sales content

Factory CRO

We are proud to offer our early-detection program designed to help medical device companies correct poorly designed clinical trials, effectively saving the study from ultimately being rejected by FDA or European regulators.

U.S.A

Virtual Booth

Digital Content

INTERNATIONAL CLINICAL TRIAL RESCUE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

TFS International AB

Sweden

Virtual Booth

The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

INTERACTION WITH REGULATORY AGENCIES WORLD-WIDE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Greenleaf Health Inc

U.S.A

Virtual Booth

Greenleaf Health Inc. offers various services such as: Analysis of FDA policies and processes; User fee requirements; Advisory committee analysis; Implementation of new FDA legislation, regulations, guidance documents and FDA standard operating procedures.

REGULATORY POLICY GUIDANCE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Reliance Clinical Testing Services, Inc

RCTS offers complete clinical testing services for topical drugs and medical devices. Our team has extensive experience in the design and execution of protocols to support the safety and therapeutic benefits of topical drugs and devices across numerous therapeutic areas.

U.S.A

Virtual Booth

Digital Content

PHARMACEUTICAL & MEDICAL DEVICE TESTING

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Medical Devices

ASK
US

Upload
your Marketing & Sales content

PAREXEL International Corporation

U.S.A

Virtual Booth

During study design, it’s critical to to optimize protocol design and global placement to achieve predictable delivery and avoid amendments that slow the process. After all, 55% of trial delays happen at the site level[1], which can have a cascade effect downstream. PAREXEL's ForeSite™

SIMPLIFY STUDY DESIGN

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Clinical Trial Design

ASK
US

Upload
your Marketing & Sales content

KAI Research

U.S.A

Virtual Booth

Our long experience in validating clinical studies has allowed us to strengthen internal procedures to maximize accountability, systematic feedback, and quality control in all aspects of studies and data handling.

QUALITY ASSURANCE OF TRIALS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

Chiltern International Ltd

We have an exceptional depth of knowledge in cardiovascular, ophthalmology, oncology, orthopedic, respiratory and women’s health applications of medical devices. Over the last three decades, our medical device study team has successfully managed hundreds of studies for all classes of medical

United Kingdom

Virtual Booth

Digital Content

MEDICAL DEVICE & DIAGNOSTICS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Medical Devices

ASK
US

Upload
your Marketing & Sales content

Greenleaf Health Inc

U.S.A

Virtual Booth

Greenleaf provides regulatory analysis for strengthening: Corporate quality systems; Corporate training programs; Corporate compliance strategies; Inspection readiness; Corporate quality and compliance organization

ANALYSIS & EXPERT CONSULTATION

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

TransPerfect

U.S.A

Virtual Booth

TransPerfect has developed Trial Interactive–the world's only clinical trial solution specifically designed to meet the needs of life sciences. Now, companies that are participating in licensing activities can securely share confidential product development information through an easy-to-use,

DUE DILIGENCE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

MPI Research Inc

The medical device expertise available at MPI Research offers pharmaceutical and biotechnology companies leading-edge experience, efficiency, and precision.

U.S.A

Virtual Booth

Digital Content

MEDICAL DEVICE EVALUATION

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Medical Devices

ASK
US

Upload
your Marketing & Sales content

TFS International AB

Sweden

Virtual Booth

The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

ORPHAN DRUG DESIGNATIONS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

MPI Research Inc

MPI Research supports the animal health industry through early stage research conducted under Good Laboratory and Good Clinical Practices (GLP, GCP). We’ve earned the trust of industry colleagues through our decades of animal health safety experience and expanded capabilities including, GCP

U.S.A

Virtual Booth

Digital Content

ANIMAL HEALTH

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Veterinary / Animal Health

ASK
US

Upload
your Marketing & Sales content

TFS International AB

Sweden

Virtual Booth

The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

PEDIATRIC INVESTIGATIONAL PLANS (PIPS)

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Greenleaf Health Inc

U.S.A

Virtual Booth

Greenleaf provides corporate insight on: FDA inspection, compliance and enforcement processes; FDA organization and structure as they relate to compliance functions and decisions; Impact of compliance-related legislation, regulations and guidance; FDA trends and priorities

REGULATORY GUIDANCE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Chiltern International Ltd

Chiltern’s Strategic Regulatory team is your end-to-end solution for navigating regulatory processes throughout your product’s life cycle. Our team uses a collaborative approach to generate a personalized strategy that aligns with your business goals and gives you the best chance of regulatory

United Kingdom

Virtual Booth

Digital Content

CLINICAL TRIAL AUTHORIZATIONS (CTA)

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

TransPerfect

U.S.A

Virtual Booth

TransPerfect’s eFeasibility solution allows investigators to populate information into a web survey, then relaying the information to the investigators. These surveys can be done completely online or they can be printed out and done in hard copy, and uploaded via email or fax upon preference.

EFEASIBILITY

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Factory CRO

Our extensive experience and knowledge can help you plan a optimal study design. In addition to our internal expertise, you can get direct market feedback through meetings with panels of clinical experts. Let us be your bridge to the key opinion leaders and surgical experts throughout Europe.

U.S.A

Virtual Booth

Digital Content

PROTOCOL / STUDY DESIGN

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Clinical Trial Design

ASK
US

Upload
your Marketing & Sales content

Chiltern International Ltd

Chiltern’s Strategic Regulatory team is your end-to-end solution for navigating regulatory processes throughout your product’s life cycle. Our team uses a collaborative approach to generate a personalized strategy that aligns with your business goals and gives you the best chance of regulatory

United Kingdom

Virtual Booth

Digital Content

IND / IDE / BLA APPLICATIONS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Factory CRO

Factory’s team has a broad and in depth knowledge on FDA requirements and procedures and can help you design a regulatory strategy specific for your device.

U.S.A

Virtual Booth

Digital Content

FDA REGULATORY STRATEGY

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

Greenleaf Health Inc

U.S.A

Virtual Booth

Greenleaf provides training and development for: Issuing technical reports, determining policies and procedures, and revising company SoPs; Preparing for FDA meetings and facilitating effective interactions with FDA; etc.

CORPORATE TRAINING & DEVELOPMENT

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Training

ASK
US

Upload
your Marketing & Sales content

MPI Research Inc

MPI Research is known for its on-time delivery in meeting the IND and NDA submission filing goals of its Sponsors. We have substantial experience conducting studies in accordance with domestic and international regulatory agencies, including FDA, EPA, USDA, OECD, ICH, and JMHW.

U.S.A

Virtual Booth

Digital Content

REGULATORY RECORD

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Celerion

U.S.A

Virtual Booth

Celerion consults in the scientific and regulatory phases of biopharmaceutical product development. Our scientists are very engaged in the practical interpretation of the requirements for biosimilar drugs emerging in Europe.

BIOPHARMACEUTICAL DEVELOPMENT

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Biopharmaceuticals

ASK
US

Upload
your Marketing & Sales content

Factory CRO

Controlling development timelines and budgets are essential for companies that want to bring a medical device to the market. Factory’s control systems give you all the information you need to keep you informed and stay in control of the process, every step of the way.

U.S.A

Virtual Booth

Digital Content

TIMELINES & BUDGETARY CONTROL

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Chiltern International Ltd

Chiltern’s Strategic Regulatory team is your end-to-end solution for navigating regulatory processes throughout your product’s life cycle. Our team uses a collaborative approach to generate a personalized strategy that aligns with your business goals and gives you the best chance of regulatory

United Kingdom

Virtual Booth

Digital Content

PRODUCT LABELING TESTING

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

Greenleaf Health Inc

U.S.A

Virtual Booth

Greenleaf provides evaluation and response recommendations for: Facility and supply chain audit reports; cGMP deficiency letters; Establishment inspection reports (EIRs)nFDA Form 483s; Warning letters; Untitled letters; Other compliance- and enforcement-related actions.

FDA COMMUNICATIONS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

PPD

U.S.A

Virtual Booth

PPD's clinical quality assurance (CQA) services help our clients ensure the integrity of their clinical trials. We advise clients on how to verify the integrity of scientific data and ensure adherence to protocols and international regulatory guidelines. We also help clients protect research

CLINICAL QUALITY & COMPLIANCE SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

Factory CRO

We would be happy to provide a free consultation about your European regulatory strategy, without any future obligation. We can assist with Notified Body selection and negotiations.

U.S.A

Virtual Booth

Digital Content

EUROPEAN REGULATORY STRATEGY

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

Chiltern International Ltd

Chiltern’s Strategic Regulatory team is your end-to-end solution for navigating regulatory processes throughout your product’s life cycle. Our team uses a collaborative approach to generate a personalized strategy that aligns with your business goals and gives you the best chance of regulatory

United Kingdom

Virtual Booth

Digital Content

REIMBURSEMENT

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Nutrasource

Our regulatory team stays abreast of ever changing regulations in the North American market. Our clients have diverse portfolios often crossing different regulatory categories.

Canada

Virtual Booth

Digital Content

REGULATORY APPLICATIONS & PRODUCT APPROVALS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Chiltern International Ltd

Chiltern’s Strategic Regulatory team is your end-to-end solution for navigating regulatory processes throughout your product’s life cycle. Our team uses a collaborative approach to generate a personalized strategy that aligns with your business goals and gives you the best chance of regulatory

United Kingdom

Virtual Booth

Digital Content

SAFETY RISK MINIMIZATION PLANS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

PPD

U.S.A

Virtual Booth

With more than 25 years of experience, PPD brings diverse expertise across therapeutic areas and functional disciplines to provide biopharmaceutical consulting services throughout the product life cycle.

PPD CONSULTING SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

TFS International AB

Sweden

Virtual Booth

At TFS we strive to ensure costs are kept within the budget using our in-depth knowledge of international and local regulatory requirements and our network of global investigators to ensure that the trial objectives will be met on time.

GLOBAL QA & COMPLIANCE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

Chiltern International Ltd

Chiltern’s Strategic Regulatory team is your end-to-end solution for navigating regulatory processes throughout your product’s life cycle. Our team uses a collaborative approach to generate a personalized strategy that aligns with your business goals and gives you the best chance of regulatory

United Kingdom

Virtual Booth

Digital Content

SCIENTIFIC ADVICE, PROTOCOL ASSISTANCE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Chiltern International Ltd

Chiltern’s Strategic Regulatory team is your end-to-end solution for navigating regulatory processes throughout your product’s life cycle. Our team uses a collaborative approach to generate a personalized strategy that aligns with your business goals and gives you the best chance of regulatory

United Kingdom

Virtual Booth

Digital Content

SUITABILITY FOR REGISTRATION

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

TransPerfect

U.S.A

Virtual Booth

TransPerfect LMS can help you assist with meeting your global regulatory training requirements.

LEARNING MANAGEMENT SYSTEMS (LMS)

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Training

ASK
US

Upload
your Marketing & Sales content

TransPerfect

U.S.A

Virtual Booth

eCTD preparation and review, global CTA submissions, Packaging and labeling translation

REGULATORY CONSULTING SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Celerion

U.S.A

Virtual Booth

Leveraging our regulatory experience and familiarity with the tobacco industry, allows us to assist clients as they navigate the evolving regulatory pathway toward product approval.

GLOBAL REGULATORY SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Tobacco

ASK
US

Upload
your Marketing & Sales content

Nutrasource

Our regulatory team stays abreast of ever changing regulations in the North American market. We take the stress out trying to understand the differences in regulations, classification and requirements between Canada and the United States.

Canada

Virtual Booth

Digital Content

CLINICAL REGULATORY AFFAIRS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

PPD

U.S.A

Virtual Booth

Clients can accelerate the process of bringing their new products to market with the experience, resources and global reach of PPD’s medical device development team.

MEDICAL DEVICE DEVELOPMENT INDUSTRY EXPERTISE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Medical Devices

ASK
US

Upload
your Marketing & Sales content

Chiltern International Ltd

Over the last three decades, our medical device study team has successfully managed hundreds of studies for all classes of medical products.

United Kingdom

Virtual Booth

Digital Content

REGULATORY CONSULTING

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

PAREXEL International Corporation

U.S.A

Virtual Booth

PAREXEL's Education Services offers flexible, customizable and end-to-end technology training and training compliance solutions to increase clinical trial and regulatory performance.

PAREXEL'S EDUCATION SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Training

ASK
US

Upload
your Marketing & Sales content

TFS International AB

Sweden

Virtual Booth

TFS Quality Assurance (TFSQA), an independent group within TFS, is responsible for ensuring the quality of the work provided by TFS, and that all work is conducted in compliance with applicable GxP guidelines, relevant regulatory requirements and applicable Standard Operating Procedures (SOPs).

QUALITY ASSURANCE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Quality & Compliance

ASK
US

Upload
your Marketing & Sales content

PAREXEL International Corporation

U.S.A

Virtual Booth

PAREXEL Consulting overcomes the obstacles to get products to market faster and smarter. Our scientific, regulatory, and operational expertise puts best practice standards to work for clients large and small, designing solutions for a constantly evolving healthcare landscape.

YOUR STRATEGIC GUIDE IN PRODUCT DEVELOPMENT

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Prague Scientific

Czech Republic

Virtual Booth

From early-stage development through the approval and launch of new products, Prague Scientific's regulatory experts can assist with all regulatory needs across the entire product lifecycle.

REGULATORY SUPPORT

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Overview

ASK
US

Upload
your Marketing & Sales content

Navitas Inc

At Navitas we take a personalized approach to each client situation to ensure results are grounded in industry best-practices, but tailored to specific needs, fit-for-purpose, cost-effective, scalable, and compliant.

U.S.A

Virtual Booth

Digital Content

STRATEGIC CLINICAL CONSULTING

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Dalmia

DRDL is providing an effective strategy of Pharmaceutical APIs, Finished Formulation and New medical device registration in India with the help of our network partner in the segment.

India

Virtual Booth

Digital Content

REGULATORY AFFAIRS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Clinica Research Solutions

CLINICA provides support for drug development partners to overcome hurdles related to clinical requirements of the DCGI, FDA, EMA, & other regulatory authorities. It offers preparation of regulatory packages, CTRI registration, product registration, etc.

India

Virtual Booth

Digital Content

CLINICAL TRIAL REGULATORY SUPPORT

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Overview

ASK
US

Upload
your Marketing & Sales content

Dalmia

Launch your Medical Device in the market with DRDL. We have built the absolute roadmap by keeping in view the FDA, EMA and other necessary regulations. Where, we are keeping a top view on the data monitoring, safety and risk-management.

India

Virtual Booth

Digital Content

MEDICAL DEVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Medical Devices

ASK
US

Upload
your Marketing & Sales content

Azidus Laboratories

India

Virtual Booth

Azidus offers preparation of regulatory dossiers for semi-regulated & regulated markets, preparation of dossiers in CTD format for Market Authorization in various countries, review & preparation of all modules of CTD for regulatory submission.

REGULATORY SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Arcinova

United Kingdom

Virtual Booth

We offer regulatory & consultancy services to support our clients at every stage of their project whether you require help preparing regulatory dossiers or data assessment.

REGULATORY CONSULTING SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

ICBio Clinical Research Pvt Ltd

ICBio being one of the best CRO in India provides regulatory services to facilitate all stages of drug development. We provide a wide range of Regulatory Writing Services & project management services across clinical & post marketing stages.

India

Virtual Booth

Digital Content

REGULATORY AFFAIRS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

ICBio Clinical Research Pvt Ltd

We do offer Dossier compilation as per Asean Common Technical Dossier (ACTD), Common Technical Dossier (CTD) Guidelines, Drug Master File. We draft data for BMR, MFR, Process & Analytical Validation, Stability Study reports, COA & related reports.

India

Virtual Booth

Digital Content

DOSSIER DEVELOPMENT (CTD / ECTD)

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Overview

ASK
US

Upload
your Marketing & Sales content

Nuvisan GmbH

Germany

Virtual Booth

Nuvisan provides a wide range of regulatory services such as Regulatory Support to Clinical Trials (IMPDs, Preparation & submission of CTAs) Regulatory Strategy & Development, Preparation of Application Dossiers in CTD format.

REGULATORY SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Navitas Inc

Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

U.S.A

Virtual Booth

Digital Content

REGULATORY CONSULTING

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Prorelix Research

ProRelix’s regulatory & pharmacovigilance services include clinical sections of common technical documents (CTDs) & new drug applications (NDAs), risk management plans, periodic safety update reports (PSUR) along with benefit risk evaluation reports.

India

Virtual Booth

Digital Content

REGULATORY & PHARMACOVIGILANCE SERVICES

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

Cliantha Research

Cliantha Research offers comprehensive services including regulatory submissions, phase II-III clinical trials, feasibility studies, project management, site management, data management and statistics.

India

Virtual Booth

Digital Content

REGULATORY SERVICES FOR CLINICAL TRIALS

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Regulatory Affairs

ASK
US

Upload
your Marketing & Sales content

RegPak BioPharma

RegPak has extensive experience of the preparation, submission and approval process for clinical trial applications in major clinical trial conducting countries.

Netherlands

Virtual Booth

Digital Content

CLINICAL CONSULTANCY

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Navitas Inc

Navitas Life Sciences consultants which bring over 100 years of combined experience, serve as trusted advisors, providing strategic counsel backed by years of experience, industry benchmarks and insights.

U.S.A

Virtual Booth

Digital Content

STRATEGIC REGULATORY CONSULTING

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials

Upload your Marketing & Sales content on your company Virtual Booth, click HERE

Sub Category: Consulting Services

ASK
US

Upload
your Marketing & Sales content

Navitas Inc

At Navitas, we have worked with companies to ensure medical decisions are consistent throughout the business enabling them to approach external stakeholders with a single voice.

U.S.A

Virtual Booth

Digital Content

MEDICAL GOVERNANCE

PDF Supplier PDF

URL Supplier Web Content

LM Capability #LearnMore

- Service Details

- Directory Listing

Pharma Service: Clinical Trials