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Royal Maxim Palace Kempinski

Oct 14, 2019 8:00 AM - Oct 15, 2019 5:00 PM

1st Settlement, Eastern Ring Road, New Cairo, 11477, Egypt

DIA Pharmacovigilance Workshop (Middle East & Africa Region)

Keeping up-to-date with the pharmacovigilance landscape in MENA region.

Overview

In a rapid changing environment, pharmacovigilance plays a key role in maintaining the focus on patient safety. Middle East & Africa Regions are gaining more space in the pharmaceutical landscape with the innovation and development of new medicines.

This workshop’s aim is to bring together key stakeholders from different regions to share good practices and requirements into getting the actual guidelines into practice.

The conference format is designed to stimulate dialogue and generate solutions through a series of interactive sessions and workshops conducted in an informal setting allowing for in-depth discussion in smaller groups.

Featured topics

  • Signalling and emerging safety issues
  • Inspections
  • Risk Management Plan
  • PSMF: general developments
  • Sub-standards and Counterfeit Medicines
  • Paediatric PV Guidelines

Who should attend?

Established professionals who are seeking to increase their network of like-minded colleagues; share their thoughts and practices with others; learn the most current regulatory views and gain practical knowledge in key areas in pharmacovigilance, including:

  • Signal management
  • Risk Management Planning
  • PSMF maintenance
  • Clinical Trials

Professionals involved in:

  • Drug Safety/Pharmacovigilance
  • Risk Management, including Risk Evaluation and Mitigation Strategies (REMS)
  • Benefit-risk assessment and communication
  • Medical Product Safety Assessment
  • Regulatory Affairs
  • Clinical Trials
  • Pharmaceuticals, biologics, combination products, devices
  • Clinical Research and Clinical Research Organizations
  • Health Outcomes
  • Academic Research Centers
  • Regulatory Agencies 

Learning objectives

  • Seek direct answers to the business challenges you are facing every day
  • Understand how other organisations are managing through the shift of sharing all information to sharing relevant information
  • Ensure that your pharmacovigilance work matches up with inspector expectations, and delivers the efficient outcomes for patients.    

Program Committee

  • Shahinaz  Badr
    Shahinaz Badr Pharmacovigilance Consultant and PVQA Auditor - EMEA
    Pharma Quality Europe, United Arab Emirates
  • Sean  Burke, MSc
    Sean Burke, MSc Pharmacovigilance Lead, EEMEA
    Merck , United Kingdom
  • Dana  Isleem
    Dana Isleem Pharmacovigilance Manager
    Bristol-Myers Squibb , Saudi Arabia
  • Raghda  Mohamed
    Raghda Mohamed Patient Safety Cluster Lead - Middle East and Turkey
    Takeda, United Arab Emirates
  • Shanthi  Pal, DrSc, MPharm
    Shanthi Pal, DrSc, MPharm Group Lead, Medicines Safety, Safety & Vigilance
    WHO, Switzerland
  • Reem K Al Essa, MBA
    Reem K Al Essa, MBA Coordination & Development Superintendent Pharmaceutical Services Administration
    Ministry of Health, Kuwait
  • Sultana  Essa Omar Ali Bin Haider
    Sultana Essa Omar Ali Bin Haider Pharmacovigilance Officer, Drug Department
    Ministry of Health & Prevention, United Arab Emirates
  • Nadjat  LOUMI-MEDEDJEL
    Nadjat LOUMI-MEDEDJEL Directrice Générale
    Centre National De Pharmacovigilance et De Matériovigilance (CNPM), Algeria
  • Manal  Younus
    Manal Younus Head of Iraqi Pharmacovigilance Centre, Directorate of Technical Affairs
    Ministry of Health, Iraq
  • Hadir  Rostom
    Hadir Rostom Head, Egyptian Pharmaceutical Vigilance Center (EPVC)
    Pharmaceutical Affairs Central Administration (CAPA), Ministry of Health, Egypt, Egypt

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