Regulatory services In Morocco for the pharmaceutical industry are overseen by the Moroccan Ministry of Health (Ministère de la Santé) and the Moroccan Medicines and Pharmacy Agency (Agence du Médicament et de la Pharmacie, AMPP).These agencies are responsible for ensuring the safety, efficacy, and quality of pharmaceutical products in the country. Key regulatory services include:
Drug Registration: The AMPP evaluates and approves new medicines for marketing in Morocco, ensuring they meet safety, efficacy, and quality standards.
Good Manufacturing Practice (GMP): Enforcing GMP guidelines to ensure that pharmaceutical products are produced and controlled to the highest standards.
Pharmacovigilance: Monitoring...
Regulatory services In Morocco for the pharmaceutical industry are overseen by the Moroccan Ministry of Health (Ministère de la Santé) and the Moroccan Medicines and Pharmacy Agency (Agence du Médicament et de la Pharmacie, AMPP).These agencies are responsible for ensuring the safety, efficacy, and quality of pharmaceutical products in the country. Key regulatory services include:
Drug Registration: The AMPP evaluates and approves new medicines for marketing in Morocco, ensuring they meet safety, efficacy, and quality standards.
Good Manufacturing Practice (GMP): Enforcing GMP guidelines to ensure that pharmaceutical products are produced and controlled to the highest standards.
Pharmacovigilance: Monitoring and evaluating the safety of pharmaceutical products after they are marketed, including the collection and analysis of adverse drug reactions.
Inspection and Licensing: Conducting inspections of manufacturing facilities, distribution networks, and pharmacies, and issuing licenses for pharmaceutical activities.
Pricing and Reimbursement: Regulating the pricing of pharmaceuticals and determining reimbursement rates for medicines under the national healthcare system.
These services help ensure that medicines available in Morocco are safe and effective for public use.
