Department of Regulatory Affairs & Pharmacovigilance
Handles all activities related to registering medicines, medical devices, cosmetics, body care products, and food supplements, ensuring regulatory compliance throughout the process.
Department of Regulatory Affairs
- The Regulatory Affairs & Pharmacovigilance Department oversees all activities related to registering medicines, medical devices, cosmetics, body care products, and food supplements. It focuses on managing regulatory processes, monitoring product life cycles, and ensuring compliance and enforcement throughout.
Pharmacovigilance
Pharmacovigilance, as defined by WHO, involves detecting, recording, assessing, and understanding adverse drug reactions or other safety issues associated with medicines. It aims to maximize the benefits and minimize the risks of medicine use, promoting safer, more effective, and rational use.
The mission of Pharmacovigilance and Health Product Surveillance at Laboratório Edol is to systematically collect and process safety information related to our medicines, medical devices, cosmetics, body care products, and food supplements. We adhere to ethical and quality procedures to provide health professionals and patients with accurate and up-to-date safety information on our products.