The third International Forum of Pharmaceutical Inspectorates (IFPI) will provide an online attendance option for the national regulatory authorities, GMP professionals, and pharmaceutical industry representatives from around the world.
The Forum will kick off with the opening ceremony, followed by a Plenary Session focused on implementing Good Regulatory Practice (GRP). The event agenda will also offer Expert and Information sessions.
Key discussion topics will include:
• regulation and manufacture of ATMPs, blood products, and radiopharmaceuticals;
• best-practice exchange on planning and carrying out inspections, including inspections of sterile products;
• reducing administrative barriers when introducing medicines to the market.
For more details and to register, please email: info@ifpi-forum.com
The Forum will kick off with the opening ceremony, followed by a Plenary Session focused on implementing Good Regulatory Practice (GRP). The event agenda will also offer Expert and Information sessions.
Key discussion topics will include:
• regulation and manufacture of ATMPs, blood products, and radiopharmaceuticals;
• best-practice exchange on planning and carrying out inspections, including inspections of sterile products;
• reducing administrative barriers when introducing medicines to the market.
For more details and to register, please email: info@ifpi-forum.com