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PV-MI Integrated Solutions

by | Oct 3, 2025

One system. One process. One partner. Although pharmacovigilance (PV) and medical information (MI) are deeply interconnected, managing them separately often results in slower processes, duplicated work, and added regulatory pressure. For global pharma and biotech,...

CSV For Pharmacovigilance Systems

by | Jun 2, 2023

Home 9 Page Category: Pharmacovigilance CSV For Pharmacovigilance Systems So you can focus on your product development. That’s why. Dedication in pharmacovigilance. To provide optimized CSV solutions. At Biomapas, we understand the importance of compliance...

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...

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...

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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