2013

The launch of Clinical Safety and Medical Monitoring services

2012

Biomapas completes the ISO 9001:2008 to ensure high-quality services for its clients.

2011

Biomapas adds Medical Devices services to its portfolio and completes first projects.

2009

The Regulatory Affairs department is established.

2005

The Pharmacovigilance department is established.

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.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information