Zdrowie i gospodarka · 25/09/2017

FDA Hosts Public Workshop on Clinical Trial Requirements and Regulations

The US Food and Drug Administration (FDA) is hosting a public workshop to educate clinical research professionals about FDA's clinical trial requirements, regulations, and compliance with Good Clinical Practice (GCP). The event aims to facilitate interaction between FDA representatives and clinical trial staff, investigators, and institutional review boards (IRBs) to ensure informed consent and regulatory compliance.