Our Story
Farbridge Pharma Consulting is a leading expert in GxP Quality Assurance, Regulatory Affairs and Pharmacovigilance, distinguished by a proven record of excellence across Preclinical and Clinical Trials, Manufacturing, Distribution, and Patient Safety.
Founded in 2017 by a European Qualified Person living in the US, and with offices on both sides of the Atlantic, the Company is strategically positioned to serve as a bridge for Life Sciences companies to establish, maintain and oversee activities in Europe and in the United States in compliance with applicable pharmaceutical regulations. It was founded with a singular vision: to harness our extensive expertise and specialized knowledge acquired over the years in medicine and medical device-related regulations globally. Through our team of multilingual local experts, we aim to facilitate seamless access for our clients to foreign clinical trials and markets.
Our strengths
We have Quality experts in all the pharmaceutical Good Practices on both sides of the Atlantic:
- GMPGood Manufacturing Practices
- GCPGood Clinical Practices
- GVP or GPvPGood Pharmacovigilance Practices
- GLPGood Laboratory Practices
- GDPGood Distribution Practices
- GTPGood Tissue Practices
- GPPGood Production Practices (medicinal cannabis)
- GACPGood Agricultural and Collection Practices (medicinal cannabis)
The majority of our consultants are based in the US and in Europe, but over the years and driven by clients’ requests, we have expanded our network of auditors to other areas of the world such as Canada, Brazil, South Africa, Australia, Japan, India and China.