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Overview

Topics will include:

Current Regulatory Processes in the Region
Reliance pathways and accelerated approval
Regulatory coverngence internationally and regionally
Biotherapeutic & Biosimilars
Pharmacovigilance
Non-Prescription Medicines: Status and Registration
Lifecycle Management 

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Who should attend?

Representatives from Health Authorities and Professionals in:

• Regulatory Affairs
• Quality Assurance
• Clinical
• Safety
• Research & Development

And other professionals involved in or interested in the aspects surrounding
• Registration and Life Cycle Management of medicinal products and
• Regulatory convergence

Program Committee

  • Dounia   El Maimouni
    Dounia El Maimouni
    JANSSEN, France
  • Hany  Gamal
    Hany Gamal Regional Drug Regulatory Affairs Head, Middle East, Turkey & Africa
    Boehringer Ingelheim, United Arab Emirates
  • Nevena  Milisavljevic
    Nevena Milisavljevic Regulatory Policy Lead - EEMEA
    F. Hoffmann-La Roche Ltd, Switzerland
  • Myriam  Sedrati
    Myriam Sedrati Regulatory Affairs Director North and West Africa
    Merck Sharp & Dohme, Morocco
  • Anne  Grandjacquot
    Anne Grandjacquot Regulatory Affairs Manager
    Sanofi-Aventis, France
  • Janis  Bernat
    Janis Bernat Scientific Assistant
    IFPMA, Switzerland
  • Bouchra  Essaoui
    Bouchra Essaoui DRA Head
    Novartis Pharma Maroc SA, Morocco
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