Outstanding expert contributions providing essential insight:

  • beat_widler Beat Widler
    Chair of Advisory Council
    Drug Information Association, Switzerland

  • nadia Nadia Cheaib
    President
    Middle East Clinical Research Association, Lebanon

  • omar_shafey Omar Shafey
    Senior Officer, Medical Research, Public Health and Policy Department
    Health Authority Abu Dhabi, UAE

  • habib_ghedera Professor Habib Ghedira, M.D.,
    Professor of Medicine
    Faculty of Medicine, Tunis

  • amid_abu Amid Abu Hmaidan M.Sc.,
    Director Cancer Registry Office of Scientific Affairs and Research and Member of the Institutional Review Board, King Hussein Cancer Centre, Jordan

Accelerating the progress of clinical trials in the Middle East

With the increase in drug development cost and the pressure to develop drugs more quickly and cost effectively, global pharmaceutical companies are forced to rush to emerging markets to conduct clinical trials.

Middle East is projected to be one of the fastest growing markets for clinical research outsourcing based on availability of the required infrastructure, access to necessary patients, faster timelines and lower cost compared to other markets.

Clinical Trial Partnerships Summit Middle East will gather all the stakeholders from leading research sites, clinical research organisations, regulators, government organisations and pharmaceutical companies to provide strategies and knowledge on critical issues such as regulatory compliance, optimising clinical trials, overcoming clinical trials challenges and identifying business opportunities in the Middle East region.

Key benefits include:

  • Improve global competitiveness and collaboration to attract more research to the region
  • Learn how to facilitate patient enrolment in clinical trials
  • Meet all clinical outsourcing contacts and main investigators in the region
  • Understanding new e-clinical technologies to improve data quality and optimise clinical outcomes
  • Learn how to optimise efficiency and quality of your clinical trials through effective partnering
  • Ensure profitability by understanding the operation long term strategies for managing clinical trials
  • Manage clinical trials cost during the project life cycle
  • Enhance the quality and improve timelines for conducting oncology clinical trials

Who Should Attend?

Executives, senior level directors or director from the pharmaceutical, biotech, clinical research organisations and clinical investigators with responsibilities or involvement in the following areas:

  • Clinical research
  • Clinical operations
  • Clinical development
  • Global outsourcing
  • Clinical data management
  • Quality assurance
  • Research and development
  • Business systems and applications
  • Outsourcing
  • Regulations and compliance

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Testimonials

I learned a lot at this conference-the topics were interesting.
Janssen
A good mix of functional areas. For training purposes it has been enlightening.
ONO Pharmaceutical UK
Informative examples from daily practice.
Medigene AG

Solution Provider

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