Unlocking Success: The FSP Advantage in Clinical Research

Regulatory Outsourcing in the CEE Region

Benefits of Integrating Pharmacovigilance & Medical Information

Oncology trials in a shifting economical and geopolitical landscape

Setting up a pharmacovigilance system in Europe: Where to start? What to consider?

How to avoid delays in your early phase oncology trial?

Pharmacovigilance Opportunities in the MENA region

Pharmacovigilance Outsourcing

Q&A How does the conflict between UA & RU impact the pharma industry?

Regulatory Strategy in EAEU and rest of CIS Countries

eCTD Submission Different Strategies: In-house vs. Outsourcing

Effective IMPD Writing: The Quality Part

Successful Medical Device Registration in Russia: The Essentials

Affiliate Based Outsourcing Model for Regulatory Affairs: An Introduction

Medical Device Registration in Russia: Challenges and Issues

Strategic Pharmacovigilance Activities: Scalable and Tailor-made Outsourcing Models

Medical Device Registration in EAEU: New Legislation

Medical Device Registration in EAEU Different Routes & MRP (Part 2)

How to prepare for the Affiliate Based Outsourcing for Regulatory Affairs

Different Affiliate-Based Outsourcing Models for Regulatory Affairs

Smooth switch to the EAEU MA for medicinal products

Biomapas. A Global Partner to the Life Sciences Industry.

Biomapas - outsourcing in pharmacovigilance

Current Regulatory Challenges

Human virus vs. Computer virus

Biomapas Academy Graduation 2020

Regina Auškalnienė will lead Lithuanian Good Clinical Practice and Regulatory Affairs Association