1st Regional Conference on Regulatory Harmonisation

Event details

Website:
Location: Sofitel Casablanca Tour Blanche, Rue Sidi Belyout, Casablanca, 20190, Morocco, Europe
About

Overview

The 1st Regional Conference on Regulatory Harmonisation is connecting cross-country experts for collaborative discussion to improve access to medicines and therapies for the citizens and patients in the Maghreb Region.The Region is rapidly moving towards playing a major role in innovation and development of new medicines. The conference offers the opportunity for key stakeholders, including representatives from health authorities, local and multinational pharmaceutical companies, academia, and international governmental and non- governmental organisations: to exchange progressive views on key topics, and to identify focus areas for ongoing efforts aimed at increasing patient access to new and improved medicines.Issues and discussions will be addressed through the lens of Morocco, Algeria, Tunisia, World Health Organisation, and global needs as well as multidisciplinary perspectives.

4 Reasons to Attend:

  • Participate in a uniquely neutral discussion on how Algeria, Morocco, and Tunisia can play a leadership role in drug development.
  • Gain behind-the-scenes access to the future of health policy in the Maghreb region.
  • Learn best practices from global life sciences and regulatory leaders on how to address rapidly changing needs of patients.
  • Establish leading strategies and processes for getting breakthrough medicines to patients faster.

French – English translation will be available throughout the conference

Topics will include:

  • Regulatory processes in the region
  • Pre-marketing
  • Post-marketing
  • Biosimilars
  • Patient Access
  • Safety and Pharmacovigilance Management
  • Life cycle management
  • Non-prescription medicines

Who should attend?

Representatives from Health Authorities and Professionals in:
• Regulatory Affairs
• Quality Assurance
• Clinical
• Safety
• Research & DevelopmentAnd other professionals involved in or interested in the aspects surrounding
• Registration and Life Cycle Management of medicinal products and
• Regulatory convergence