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Promotional Material

by | Mar 5, 2021

Promotional and Advertising Material Review Health Authorities regulate promotional materials and activities that companies engage in or sponsor and intend to influence the prescription and use of a drug product. All promotional content should comply with...

Medicinal Product Lifecycle Management

by | Mar 5, 2021

Medicinal Product Lifecycle Maintenance Medicinal product lifecycle management is defined as the process of managing the entire lifecycle of the product. This includes its clinical development, marketing authorization and post-authorization activities. As medicinal...

Regulatory Affairs Support in EAEU Region

by | Mar 5, 2021

Regulatory Affairs Support in EAEU Region Our experts are qualified scientists with extensive experience in the pharmaceutical industry and regulatory affairs.  We provide registration procedure services in all Eurasian Economic Union countries, starting from medical...

Pharmacovigilance Audits

by | Feb 10, 2021

Pharmacovigilance Audits Biomapas offers Pharmacovigilance (PV) audits to evaluate the appropriateness and effectiveness of your pharmacovigilance (PV) system. Our well-trained auditors with a proven track record keep an objective, independent mindset when inspecting...

Pharmacovigilance

by | Feb 10, 2021

Pharmacovigilance  A partner that combines local expertise with a global reach to meet compliance requirements. Safety doesn’t happen by chance. It happens by vigilance. A solid extension of your pharma or biotech safety team for both full a PV system and a...

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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