Sarah T’Kindt

Pharm, GCP Inspector
Federal Agency for Medicines and Health Product

Sarah T’Kindt has a background as Pharmacist and is currently a good clinical practices (GCP) inspector with over more than 18 years of experience in the field of clinical trials. She was previously responsible for the approvals of clinical trials at the Belgian Federal Agency for Medicines and Health Product (FAMHP) and since 13 years she is performing GCP inspections at national level as well as for CHMP requested inspections for the European Medicines Agency (EMA). As member of the GCP Inspectors working group at EMA she was involved in the set up and the publication of the recommendation
paper on decentralised elements in Clinical Trials. 

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