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Albert Bekfi

by | Aug 30, 2021

Albert Bekfi – MSc Albert is a pharmacovigilance expert with over 11 years of experience in the field. He has vast experience in different pharmacovigilance operations, from literature monitoring, vendor management, global and local case processing oversight, to...

Egidija Paurienė

by | Apr 7, 2021

Egidija Paurienė – MD Egidija Pauriene, MD, manages and ensures quality systems. She helps guide the integration of the corporate strategies of Biomapas Group related to GxP Quality Assurance, regulatory compliance, including Good Pharmacovigilance Practice and...

Jolanta Diskaitė

by | Apr 7, 2021

Jolanta Diskaitė – MEc Jolanta has almost 20 years of HR management and Organizational Development practice in leadership positions of various international, local and public companies. She is experienced in building an organizational culture that supports...

Liudas Karnickas

by | Apr 7, 2021

Liudas Karnickas – LLM Liudas Karnickas is a qualified attorney at law and an experienced professional in regulatory compliance, data privacy, R&D/technology management and IP protection matters. For more than 15 years he actively advises the life science...

Regina Auškalnienė

by | Apr 7, 2021

Regina Auškalnienė – MD Regina Auskalniene is a Medical Doctor, cardiologist. She has over 13 years of experience in Clinical Research gained in the world-largest CRO IQVIA working in different roles like Line Manager for CRAs and CTAs in the Baltic region,...

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

Discover how Biomapas provides all the support to accelerate your clinical trials and optimize your drug development process.

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.

Quality Assurance

Export auditors help identify gaps and close them with actionable solutions. 

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