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Big enough to cover all your needs.
Small enough to care.

Your global outsourcing partner for Clinical Research, Pharmacovigilance, Regulatory Affairs and Medical Information.

These solutions might benefit you:

Built Around You.
Solutions That Deliver.

Meeting timelines and milestones is critical to move your development program forward while keeping the goal in mind.

Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization.

Clinical Research

Reliable support for every phase of your clinical trial, from recruitment to results.

Pharmacovigilance

Flexible safety monitoring to keep your products compliant and trusted.

Regulatory Affairs

Confidently navigate regulatory challenges with expert support.

Medical Information

Clear, accurate medical information 24/7, tailored for global audiences.

Exceeding
Expectations

The passion and experience of our people ensure timely execution every time. And, our team of highly educated Life Sciences professionals has a track record of exceeding our clients’ expectations.

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recurring clients

News

Biomapas Welcomes David Passov as CEO

24-02-2025

We are pleased to announce the appointment of David Passov as our new Chief Executive Officer, effective 21st February 2025.

Webinar: How Mid-Sized CROs and Site Networks Deliver Clinical Trial Success

27-05-2025, 1 PM CET

Balancing agility, reach, and patient focus in clinical trials isn’t a straightforward task. The key? The right CRO and site network partnerships. Hear from a panel of experts across CROs, global site networks, and SMOs as they share real-world insights and strategies.

Affilate-Based Outsourcing in Regulatory Affairs
Whitepaper

Discover how you can enhance your regulatory capabilities, address common challenges, and drive efficiency. Unlock the potential and download our whitepaper now.

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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.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information