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Readability User Testing 

by | Apr 25, 2025

When patients misunderstand medicine instructions, the consequences can be serious. That’s why regulators in the EU and EAEU require Readability User Testing (RUT) to ensure patients can find and understand the information they need, before mistakes happen. RUT...

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...

Affiliate Based Outsourcing

by | Apr 5, 2023

Home 9 Page Category: Regulatory Affiliate-Based Outsourcing for Regulatory Affairs So you can focus on core matters. That’s why. Make An Impact. All Across Europe. Outsourcing local activities is an attractive option because this strategic decision enables...

M&A Support

by | Apr 5, 2023

Home 9 Phase: Post Marketing M&A Support For Biotech So you can focus on core matters. That’s why. Seamless Integration. Uninterrupted Progress. We understand that mergers and acquisitions can be complex and challenging, especially when it comes to...

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...

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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