The FAMHP is the competent authority in areas relating to the different phases of the life cycle of medicines and health products.
Their key activities apply to all medicines and health products for human and veterinary use and can be divided into four areas :
🔹 Advising partners, healthcare professionals, industry, the press, patients, as well as national, European, and global organisations.
🔹 Issue official documents such as authorisations, approvals and certificates.
🔹 Ensuring quality, safety and efficacy, in particular by carrying out inspections and controls. The FAMHP also monitors reports of suspected adverse reactions and incidents involving medicines and health products, assesses them and takes appropriate corrective action.
🔹 Take sanctions such as imposing an administrative fine; withdrawing or adapting official documents; taking a health measure; or banning.
To know more about it : https://www.afmps.be/fr/a_propos_de_lafmps/a_propos_de_lafmps/nos_activites_cles
