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Virtual

13 oct 2025 9:30 a.m. - 15 oct 2025 4:00 p.m.

(W. Europe Standard Time)

Middle East & Africa Conference (MEA)

Dive into three impactful days of knowledge-sharing, innovation, and collaboration at the virtual MEA conference from 13–15 October.

Perspectiva general

For the first time, this conference will convene key stakeholders from both the Middle East and Africa to facilitate meaningful collaboration and the development of practical solutions to shared regulatory challenges within the healthcare sector. This virtual summit signifies the beginning of an ongoing engagement between the two regions, which will be further advanced at the in-person conference scheduled for 2026.

The DIA Middle East & Africa Conference 2025 will provide a secure and inclusive platform for regulatory authorities, industry leaders, academics, and patient representatives to exchange insights and advance health outcomes. A defining feature is the active involvement of regulatory agencies from the Middle East, Africa, and beyond, with structured discussions enabling direct engagement, promoting transparency, and addressing regulatory challenges throughout the medicine lifecycle.

Key topics include regional regulatory developments, reliance, digitalisation, pharmacovigilance, and innovation.

Why you should attend:

  1. Collaborate with Health Authorities’ representatives and key Industry leaders from the various countries in the MEA region and contribute to shaping the future of the regulatory landscape in the region.
  2. Connect with 300+ participants, representing all countries in the Middle East and Africa regions and beyond.
  3. Discuss new strategies and processes to be implemented in the Middle East and Africa regions.
  4. Learn how reliance, harmonisation initiatives and collaboration contribute to an efficient and sustainable regulatory system in the Middle East and Africa regions.

Who will you meet?

  • Regulatory Authorities’ representatives from the region and beyond.
  • Experts from international organisations.
  • Thought leaders, global and local stakeholders from both local and global organisations.

Temas destacados

  • Regional Regulatory Science Developments
  • International Collaboration & Reliance
  • Regulatory Systems Strengthening
  • Medecines Lifecycle Management
  • Bringing Innovation to the MEA region
  • Capacity building for local manufacturing
  • The MEA region as a Clinical Trials Hub
  • Digital Transformation of the Regulatory Systems
  • Use of AI in the Medicinal Products Development Lifecycle
  • Orphans Drug Designations & Rare diseases policies and designation
  • Advanced Therapies
  • Patient Engagement throughout the lifecycle

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DIA Middle East and Africa Conference

¿Quiénes deben asistir?

The conference is directed at key stakeholders that are active or are interested in these diverse and changing regions, including representatives from Regulatory Agencies, Ministries of Health, and local and global pharmaceutical companies.

 

Need Approval in Order to Attend?

Download and fill out our justification letter to advocate to your supervisor why this is a must-attend event.

Download letter (CLICK HERE)

 

Comité del programa

  • Ali  Al Shibly Murad
    Ali Al Shibly Murad Chair - Lebanese Regulatory WG; Regulatory Affairs Senior Specialist -Levant
    MSD, Lebanon
  • Abdulrahim  Alyahya
    Abdulrahim Alyahya SaudiArabia Regulatory WG; Director-Regulatory Policy, Governmental Affair & TSO
    Biogen, Saudi Arabia
  • Dorra  Idir
    Dorra Idir Chair-Tunisia Local Network WG & Chef de département affaires réglementaires PPP
    Sanofi Aventis Tunisia, Tunisia
  • Mounay Hussein Khafaja, PharmD, MSc
    Mounay Hussein Khafaja, PharmD, MSc Chair-Iraqi RegulatoryWG; Regulatory Affairs Director & Reg.Center of Excellence
    Merck (MSG), Lebanon
  • Alia  Seoud Abdalla
    Alia Seoud Abdalla Global Regulatory Sciences Head (Africa Cluster)
    Pfizer, Egypt
  • Amira Deia Younes
    Amira Deia Younes Director-Eastern Europe, Middle East & Africa (EEMEA) Global Regulatory Policy
    MSD, United Arab Emirates
  • Asma  Messai
    Asma Messai License To Operate Enabler, Tunisia and Libya
    Roche, Tunisia
  • Dalia  Fouad
    Dalia Fouad Middle East Region Head - Global Regulatory Affairs
    Sanofi Aventis, United Arab Emirates
  • Deema  Al Naji
    Deema Al Naji Director, African Cluster & MEA Regulatory Policy Lead
    AstraZeneca, United Arab Emirates
  • Dina  Fathy, MPharm, AHIP
    Dina Fathy, MPharm, AHIP Senior Director, Regulatory Affairs Middle East Subregional Lead
    MSD UAE, United Arab Emirates
  • Imane  Hattami
    Imane Hattami Therapeutic Area Head and Regulatory Policy Intelligence MEAR
    Abbvie Biopharmaceuticals Gmbh, Morocco
  • May  Shawky Mohamed
    May Shawky Mohamed Regional Manager Regulatory Affairs MEAR
    Merck Group, United Arab Emirates
  • Melly  Lin, MS
    Melly Lin, MS CMC Regulatory Policy Lead, Pharma Technical Regulatory
    F. Hoffmann-La Roche Ltd, Switzerland
  • Neveen  Kamel
    Neveen Kamel Regulatory Affairs Head North Africa, Egypt & French-speaking Africa
    Merck Group, Egypt
  • Niveen  Osman, MBA
    Niveen Osman, MBA Regulatory Affairs Director Middle East & Africa
    Amgen Inc., United Arab Emirates
  • Patricia  Salami
    Patricia Salami Senior Director, Regional RA Head - MEAR (Middle East_Africa_Turkey_Russia_CIS)
    Merck, United Arab Emirates
  • Sara  Torgal, MPharm
    Sara Torgal, MPharm Global Regulatory Policy Lead
    DIA, Switzerland
  • Zainab  Aziz, MSc, RPh
    Zainab Aziz, MSc, RPh IFPMA ARN Co-Chair & Associate Director, Regulatory Policy Middle East & Africa
    Novartis, South Africa

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