Medical Devices (EU)

by | Jul 5, 2022

Home 9 Page Category: Pharmacovigilance Medical Device & IVD Services in the EU Medical Device & IVD Experts. To take your product from idea to CE. Biomapas’ local experts can provide you with regulatory Medical Device Services in the EU to take you...

Local Regulatory Affairs Support

by | Mar 4, 2022

Home 9 Page Category: Regulatory Local Regulatory Affairs Support Insource our Local Regulatory experts. When and where you need them the most. Product lifecycle management is a challenge for Marketing Authorization Holders in a highly competitive market and a...

Marketing Authorization

by | Mar 21, 2021

Marketing Authorization With a strong presence across Eastern Europe and the CIS region we can accelerate your Clinical Development where patient recruitment is fast and reliable, and investigators are keen to participate in trials. Development Marketing Authorization...

Safety Database – Veeva Vault

by | Mar 21, 2021

Home 9 Page Category: Pharmacovigilance Drug Safety Database – Veeva Vault Veeva has the ambition to become the largest provider of drug safety databases in the upcoming years, leaving other well-known providers such as Aris Global and Oracle ARGUS behind. ...

Pharmacovigilance Database

by | Mar 10, 2021

Home 9 Phase: Marketing Authorization Pharmacovigilance Database Biomapas pharmacovigilance and clinical safety management services are supported by a fully E2B and CFR21 Part 11 compliant database. Our safety database has an integrated submission management tool...

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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

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