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DIA to Host 10th Middle East Regulatory Conference
Date:9/10/2013

lopments in the European Union (EU), World Health Organization and Middle Eastern region as well as falsified medicines.
  • The Concept of Biotech Medicine and Biosimilars—Updating biosimilar requirements and assessments.
  • Global Health Economics and Market Access—Discussing faster and better accessibility to medicines for patients.
  • Regulatory Life Cycle Management—Optimizing maintenance and product compliance.
  • Regulatory Data Exclusivity and Patents—Educating stakeholders on the data protection landscape in the Middle East and what remains to be done.
  • Code of Ethics and Promotion—Discussing the implementation in the EU and Middle Eastern regions and sharing regulators’ and the industry’s perspectives.
  • Ministry of Health speakers include:

    • Professor Saleh A. Bawazir, vice president of drug affairs, Saudi Food and Drug Authority, Kingdom of Saudi Arabia
    • Dr. Bahaa Eldin Fateha, chief executive, National Health Regulatory Authority, Kingdom of Bahrain
    • Mr. Thomas Heynisch, deputy head of unit, Food and Healthcare Industries, Biotechnology, European Commission, Belgium
    • Dr. Hayel Mohamad Obeidat, director general, Jordan Food and Drug Administration, Jordan
    • Dr. Colette Raidy, head, Pharmaceutical Inspection Department, Ministry of Public Health, Lebanon
    • Dr. Shahrokh Veisi, Biologics Department, Food and Drug Organization of Ministry of Health, Iran
    • Dr. Christa Wirthumer-Hoche, member, CMDh, and deputy head, Austrian Medicines and Medical Devices Agency, Austria

    To find out more about the event and to register, visit the website for DIA’s 10th MERC.

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