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Study Design and Protocol Development

by | Aug 10, 2020

Study Design & Protocol Development A well-written clinical study protocol (CSP) not only describes how a clinical trial will be conducted but ensures safety of the study subjects, integrity of the data collected and communicates the use of investigational product...

Clinical Safety

by | Jul 10, 2020

Clinical Safety Monitoring Insource our Clinical Safety experts when and where you need them the most. From Early Phase studies to large Phase III trials, our devoted colleagues contribute to guaranteeing effective safety monitoring during the execution of your...

Rescue Studies

by | Jun 16, 2020

Rescue Studies Whether your trials are in danger of not being completed on time, their quality is questionable, halted by a regulatory agency Biomapas can rescue your study. Naturally, these factors significantly affect your study timeline, regulatory filings, and...

Clinical Monitoring and Site Management

by | May 10, 2020

Clinical Monitoring & Site Management Biomapas clinical monitoring and site management offers a tailored-service approach, taking into account the individual needs of our partners and the unique characteristics of each study. Our Clinical Research Associates...

Phase II – III

by | Apr 16, 2020

Phase II – III Studies To navigate you through the complexities of Phase II and III clinical trials, we set up tailored recruitment strategies, involve medical writing specialists, and set up clinical site management throughout the process. Our dedicated...

Big Enough To Cover  All Your Needs. Small Enough To Care.

Discover the tailored solutions that Biomapas provides to accelerate your clinical trials and optimize your drug development process.
Affiliate-Based Outsourcing
CSV For Pharmacovigilance Systems
Early Phase Oncology
Functional Service Provision
M&A Support

Clinical Research

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Regulatory Affairs

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Pharmacovigilance

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Medical Information

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