This comprehensive resource provides essential guidelines and standards for regulating multisource (generic) medicines. It covers crucial areas such as prequalification of medicines, storage, distribution, and supply chain management. Additionally, it emphasizes the importance of good regulatory practices, quality management systems, and data integrity. These guidelines are essential for establishing robust regulatory frameworks, ensuring high standards in pharmaceutical quality, and combating the circulation of substandard and falsified medicines.
𝐀𝐜𝐜𝐞𝐬𝐬 𝐭𝐡𝐞 𝐟𝐮𝐥𝐥 𝐜𝐨𝐦𝐩𝐞𝐧𝐝𝐢𝐮𝐦 𝐡𝐞𝐫𝐞:
