We keep Promises. Always.

Biomapas is a functional and full outsourcing solution provider to the global life science industry.

As a trusted partner for biopharmaceutical and medical device companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory, pharmacovigilance and medical information excellence across Europe, CIS, EAEU, MENA, LATAM regions and the US throughout the entire product lifecycle. We ensure clients satisfaction by rapid, efficient and cost-effective working practices.


Early development experts to implement best-in-class strategies.

Market Authorization

Accelerating your Clinical Research in the EU and CIS regions.


Ensure you meet Post-Authorization market requirements .

Flexible solutions. Regardless of where you are in development.

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. Biomapas’ professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success.

Clinical Research

Early clinical development experts with one-stop-shop capabilities in high recruiting countries, accelerating product path to the market.

Regulatory Affairs

Local regulatory experts for Pharma, Biotech and Medical Device companies across Europe and emerging markets from dossier development to full lifecycle management.


Solid extension of Pharma and Biotech safety team for both full PV system and local safety network across Europe and emerging markets (CIS & EAEU).

Medical Information

Trusted, highly engaged MI partner, delivering excellence and ensuring compliance across Europe, CIS, and US throughout the entire product lifecycle.

The passion and experience of our people ensure timely execution every time. – Audrius Sveikata, MD, PhD. CEO & Co-Founder


Why work with us?

Our teams have comprehensive expertise and assure quality and accuracy for all our activities across a broad region. We have colleagues spread through all European, CIS, EAEU and MENA regions.

Our team of highly educated Life Sciences professionals have a track record of exceeding our clients’ expectations.

Global Reach

Recurring Customers


Getting in touch

10 + 5 =

Contact us to learn about how we can enhance your clinical development, accelerate your path to Market Authorization, and ensure compliance with local and global Post-Marketing requirements.

Or meet us at an upcoming event

World Drug Safety Congress Americas

Connect with us at the WDS to discuss your drug and medical device safety strategies.


Meet up with us to build partnerships that facilitate innovation together.

CPhI Worldwide

Join us at the leading pharma event CPhI this autumn.

SwedenBIO Summit

Connect with us at the international partnering event to discuss the advancements in the life sciences.

Recent Insights

Learn from Biomapas’ experts and let us know what you’d like to hear about!

Challenges in early phase oncology trials
Clinical Trials Regulation
Challenges in early phase oncology trials