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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...

Safety Database – Veeva Vault

by | Mar 21, 2021

A modern solution in the cloud Vault Safety is an efficient and modern drug safety solution built for today’s regulations and best practices. Biomapas Pharmacovigilance specialists utilize this powerful tool for collecting, managing, and providing real-time...

Pharmacovigilance Database

by | Mar 10, 2021

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 for direct submissions, complex search...

PSMF Development and Maintenance

by | Mar 10, 2021

PSMF Development & Maintenance A Pharmacovigilance System Master File (PSMF) summarizes your pharmacovigilance (PV) system and is a critical document for any Marketing Authorization Holder. To comply with EU PV legislation requirements, all MAHs and MAH applicants...

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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
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M&A Support

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