Case Study: International & Local Pharmacovigilance/Medical Information Services – Urgent Action

Discover how Biomapas delivered a seamless global and local transition for a pharmaceutical company, facing a critical Pharmacovigilance and Medical Information vendor transition with a non‑negotiable one‑month timeline.

In this case study, we share how Biomapas successfully supported a pharmaceutical company during a critical vendor change, delivering a seamless transition without disruption of Pharmacovigilance (PV) and Medical Information (MI) services.

Faced with a non-negotiable one‑month deadline, the client needed a partner capable of rapidly assuming both global and local PV/MI responsibilities while maintaining full compliance. We deployed an experienced, senior safety team to manage the transition, stabilise ongoing operations, and address legacy gaps across multiple markets.

The project resulted in:

  • A complete PV and MI service transition within one month
  • Global and local coverage across 16 countries
  • Uninterrupted compliance, quality, and operational continuity

Explore the case study below!

Marketing Pharmaceutical Products in CIS/Eurasian Economic Union

Marketing Pharmaceutical Products in CIS/Eurasian Economic Union

The interest of pharmaceutical companies in expanding business across the Commonwealth of Independent States (CIS) and the Eurasian Economic Union (EAEU) has been constantly growing. For the same reason, Biomapas provides end-to-end regulatory support in these...

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

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.