Virtual event | 23 May 2024

10:00 – 12:00 EST | 14:00 – 16:00 UTC | 16:00 – 18:00 CET

The European Federation of Pharmaceutical Industries and Associations (EFPIA) and the Latin America Federation for the Pharmaceutical Industry (FIFARMA) invite you to a webinar where you will hear from Regulators and industry about practical experiences, tools, and case studies that represent innovative approaches to regulatory reliance and reflect on how these learnings could be applied in Latin America and the Caribbean.

Why should you join this webinar:

• Post-approval changes (PACs) to the registered information of authorised medicinal products are introduced routinely worldwide to enhance the robustness and efficiency of the manufacturing process, ensure timely supply in case of increased demand, improve quality control techniques, respond to changes in regulatory requirements and upgrade to state-of-the-art facilities.
• Collaboration amongst Regulators has been shown to be essential to make better use of available resources and to enable more efficient regulatory pathways leading to fast access of medicines and vaccines to patients.
• Key topics will include recommendations to optimize PACs, apply regulatory reliance for the evaluation, and global pilot projects that unleashed the power of reliance for PACs.

The Webinar will be conducted in English, with translations provided in Spanish and Portuguese.

For additional information please contact us at jyothsna.krishnan@efpia.eu and diego.salas@fifarma.org