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    HTL Biotechnology is the world leader in the responsible development and production of pharmaceutical-grade biopolymers.

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    01 Compliance, Regulatory & Consulting

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    01 CLINICAL SUPPLIES MANAGEMENT HOLDINGS, INC.

    02 Covigilant LLC

    03 Evidera

    04 Factory CRO

    05 Greenleaf Health Inc

    06 MPI Research Inc

    07 Navitas Inc

    08 PAREXEL International Corporation

    09 PPD

    10 RegPak BioPharma

    11 Renejix

    12 TFS International AB

    13 TransPerfect

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    Renejix

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      CONSULTING SERVICES FOR ORAL DOSAGE FORMS

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      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.

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      Pharma Service: Clinical Trials

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      Consulting Services for Oral Dosage Forms

      Cophex 2024

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      TFS International AB

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        PRODUCT DEVELOPMENT CONSULTING

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        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

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        Evidera

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          PRAGMATIC / ADAPTIVE STUDIES

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          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.

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          MPI Research Inc

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            SUPPORTING ALL PHASES OF DRUG DEVELOPMENT

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            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

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            Covigilant LLC

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              DRUG SAFETY SOLUTIONS CONSULTATION

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

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              Greenleaf Health Inc

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                ADVISORY SERVICES

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                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

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                Evidera

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                  MARKET ACCESS

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                  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.

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                  Evidera

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                    MODELING & META RESEARCH

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                    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.

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                    CLINICAL SUPPLIES MANAGEMENT HOLDINGS, INC.

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                    CLINICAL SUPPLIES & CONSULTING

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

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                    TransPerfect

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                      DUE DILIGENCE

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                      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,

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                      Greenleaf Health Inc

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                        ANALYSIS & EXPERT CONSULTATION

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

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                        TFS International AB

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                          PEDIATRIC INVESTIGATIONAL PLANS (PIPS)

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                          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

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                          TransPerfect

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                            EFEASIBILITY

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                            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.

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                            Factory CRO

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                              TIMELINES & BUDGETARY CONTROL

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                              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.

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                              PPD

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                              PPD CONSULTING SERVICES

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                              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.

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                              PAREXEL International Corporation

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                              YOUR STRATEGIC GUIDE IN PRODUCT DEVELOPMENT

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                              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.

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                              Navitas Inc

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                                STRATEGIC CLINICAL CONSULTING

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                                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.

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                                Navitas Inc

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                                  REGULATORY CONSULTING

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                                  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.

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                                  RegPak BioPharma

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                                    CLINICAL CONSULTANCY

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

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                                    Navitas Inc

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                                      STRATEGIC REGULATORY CONSULTING

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                                      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.

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                                      Navitas Inc

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                                        MEDICAL GOVERNANCE

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                                        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.

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