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Regulatory Consultancy

by | Apr 1, 2025

Regulatory Consultancy Expert guidance for seamless approvals. Regulatory hurdles can delay or derail even the most promising drug development programs. At Biomapas, our expert regulatory consultants help pharma and biotech companies develop, refine, and execute...

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...

Patient Studies

by | Mar 23, 2021

Patient Studies We are an experienced and reliable early phase drug development services provider. Being a mid-sized CRO we are very attentive to each client and provide a close partnership with our highly motivated team; therefore, we fully adapt to our sponsor needs...

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...

Quality & Compliance

by | Mar 10, 2021

Quality & Compliance Biomapas Quality and Compliance Assurance activities help our clients to ensure the integrity of their clinical trials and protect research subjects’ rights and welfare. In addition to our internal Quality Assurance activities, we provide...

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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