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We perform Data Management & Database Programming including Study database set-up and maintenance Data Management Plan, data cleaning, coding, query issue and database lock.

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A Clinical Trial Management System (CTMS) is a software solution targeted for the Life Science industry. CTMS is commonly used to manage processes and large amounts of data involved with clinical trial management and clinical study management.

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The OTTR CompleteOrgan solution simplifies data collection, patient tracking and data management. Our software includes liver, kidney, pancreas, heart, lung, intestine and islet cell transplant solutions.

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ClinPlus Data Management (CPDM) software, our classic data management system designed to support paper-based studies, has helped clients manage clinical studies across multiple therapeutic areas and collect quality data while meeting strict timelines and budget constraints.

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AxxiTRIALS is a fully automated, unified eTMF and site investigator portal that allows regulatory document exchange between clinical trial sites and sponsors.

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Our BioVisualization service is designed to query our clinical sample databases in real-time, so your most current data is being examined. The figures are downloadable for ease of sharing with colleagues and incorporation into reporting documents.

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We perform Statistics & Statistical Programming including sample size calculation & randomization, Statistical Analysis Plan, Interpretation, tables, figures using SAS, Program/QC CDISC datasets using SAS, Define.xml & related documentation.

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At LabConnect, we’ve combined these processes with a state-of-the-art data management platform ensuring delivery of clean data according to your exact specifications. Upon study award, we will establish your global data and information management plan.

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With a highly focused staff/subject ratio, custom-designed facility for cardiac safety, and enhanced data collection processes, Spaulding Clinical is truly in a class of its own.

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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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Leveraging our industry-leading ClinPlus® eClinical software platform to manage the trial, ensure data accuracy and implement smart, proprietary algorithms to identify and mitigate risk

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LSR Trials’ custom database software is used at all sites to manage information flow.

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With the growth of next-generation therapies, you’ll need a software solution that keeps pace with evolving regulatory requirements. Our cellular therapy software includes workflow support for all hematopoietic cellular therapy products.

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You need your data rapidly to make crucial dosing decisions during a study. At Quotient, data are available in the study database within hours of collection, ready for remote sponsor access.

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With custom solutions for early- and late-phase clinical trials and a team of highly experienced project managers, DZS Clinical Services ensures that your projects are completed on schedule and within budget while complying with international quality standards.

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We provide standard operating procedure (SOP)–guided study monitoring, auditing, and quality assurance support for all phases and inpatient/outpatient studies at over 50 clinical sites for the biopharmaceutical industry and the National Institutes of Health.

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Spaulding Clinical offers a fully integrated, paperless Phase I EDC solution that redefines efficiency.

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The Goes Direct approach allows you to focus on your patients and keeps them under your direct care.

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We built more than 40 years of scientific and technical experience into our eCOA environment. Streamlined workflows and regulatory adherence make ERT eCOA easy to use with less burden for both sites and patients.

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Initially, our feasibility team develops the Synexus Delivery Plan. This provides an accurate assessment of how we plan to deliver the study with full protocol compliance, based on a medically evaluation of the protocol and any potential obstacles.

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Our statistical, pharmacokinetic and scintigraphic experts understand clinical pharmacology studies and their specialized challenges. Optimize your study objectives, design and subject numbers, and maximize your use of study data.

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The successful execution of your clinical trial hinges on the people involved day to day.

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Spaulding Clinical Research is revolutionizing the way clinical trial information is collected, analyzed, distributed, accessed, reviewed and managed - saving time and ensuring high quality study data.

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The OnQ Portal™ helps you track your study through the IRB review process, from submission to approval documents

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For each project, we develop a data management plan (DMP) that identifies the study-specific quality control steps that we will take to review the data for accuracy and completeness.

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Chiltern’s biostatistics and statistical programming team provides operational and strategic statistics for clinical research and development. Our operational expertise allows us to deliver the high-quality statistical output required for every aspect of drug development including the statistical

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TransPerfect is proud to offer Trial Interactive, our 21 CFR Part 11 compliant, web-based e-clinical solution