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

A pan-European pharma services provider rooted in the Baltics, offering worldwide Pharmacovigilance and Medical Information services and specialized Clinical Development and Regulatory Affairs capabilities.

We are proud to announce the acquisition of Delta PV, a trusted pharmacovigilance service provider headquartered in Istanbul, Turkey. This strategic move marks a key milestone in our growth journey and expands our PV capabilities, bringing us closer to our goal of building a truly global platform in life sciences services.

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

04-08-2025

We are proud to announce the acquisition of Delta PV, a trusted pharmacovigilance service provider headquartered in Istanbul, Turkey. This strategic move marks a key milestone in our growth journey and expands our PV capabilities, bringing us closer to our goal of building a truly global platform in life sciences services.

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

Balancing agility, reach, and patient focus in clinical trials requires the right partners. Hear from a panel of experts across CRO and global and emerging site networks for real-world insights on the benefits of mid-sized CRO-site partnerships.

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