The Food and Drugs Administration (FDA) regulates clinical investigations of products under its jurisdiction, such as drugs, biological products, and medical devices.

Clinical Trials and Human Subject Protection
Protecting the rights, safety and welfare of people who participate in clinical trials is a critical aspect of the FDA’s mission. FDA oversees clinical trials to ensure they are designed, conducted, analyzed and reported according to federal law and good clinical practice (GCP) regulations. FDA’s regulations and guidances for clinical trials help support efficient medical product development, while assuring trials generate the robust evidence needed to assess product safety and efficacy. The agency works to ensure its GCP policies continue to facilitate new approaches to generating quality clinical evidence.

.

Benin FDA is the National Regulatory Body to ensure the regulatory for Food Supplements, Vegetables, Foods, Herbal and Homeopathic Medicines, Drug, Veterinary Medicines, Cosmetics, Medical Devices, Household Chemical Substances, Tobacco, CBD/Hemp and Nicotine Pouch products and to make sure for a proper safety trials in general.