Research in the domain of safety of medicines and devices.

With over 20 years of experience, we are pioneers in Pharmacovigilance services in the region, offering specialized services analysis, safety and measurement of risks in the drugs, medical devices and vaccines

Nosotros

We provide effective solutions on the information about the safety of drugs and devices for growing and complex markets.

  • Our team

    The team consists of healthcare professionals, including medical doctors, qualified chemists and pharmacologists, trained nurses with master's, doctoral and post-doctoral degrees with several years of experience in various phases of clinical trials, Pharmacovigilance and Technovigilance with various national and multinational CROs and pharmaceutical companies. Our staff members are trained and constantly updated on the contemporary practices related to Pharmacovigilance and technovigilance services.

Our process consists of 5 steps to deliver concrete results on the projects.
Request for proposal from clients

Request for proposal from clients

Analysis of client´s requirements and offering possible solutions

Analysis of client´s requirements and offering possible solutions

Necessary documentation and execution of work for the client

Necessary documentation and execution of work for the client

Quality verification of the work and submission of preliminary results to the clients for any suggestions or changes

Quality verification of the work and submission of preliminary results to the clients for any suggestions or changes

Final delivery of work

Final delivery of work

Audit Calendar

Our audit calendar (internal, external agencies and clients) instills unparalleled confidence in the clients about the quality of our services.

Certification

Our Quality management system is ISO 9001:2008 by AENOR with certification number SI-0002/2017 & ISO 27001:2013 certified by AENOR with certification number ER-0315/2015.