by Anna Kamocsai | 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...
by Anna Kamocsai | Jun 10, 2020
RMP Development and Maintenance The Risk Management Plan (RMP) is the scientific document that intends to bring everything together concerning your product safety profile. This pivotal document maintains the overview of all risk, efficacy, and safety data. With our...
by Anna Kamocsai | 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...
by Anna Kamocsai | 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...
by Anna Kamocsai | Apr 10, 2020
Clinical Safety & Pharmacovigilance Our experienced team offers fast and reliable safety management plan development and smooth execution. We ensure efficient safety database set-up, including individual tenant environment set-up, specific case attributes and data...
