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Middle East and North Africa Medical Device Regulations Seminar - London, United Kingdom, June 19-20, 2019

DUBLIN, May 23, 2019 /PRNewswire/ -- The "Medical Device Regulations in the Middle East and North Africa" conference has been added to ResearchAndMarkets.com's offering.

This seminar will provide an essential overview of the key areas of requirements for product approvals for medical devices in the Middle East and North Africa.

This seminar will provide an essential overview of the key areas of requirements for product approvals for medical devices in the Middle East and North Africa. The programme will cover the regulatory requirements and developments in the individual countries. The course will include interactive discussion sessions to allow you to exchange experiences with other delegates.

Benefits of attending

  • Gain an introduction to the medical device markets: countries, numbers, economical facts and trends, regulatory environment
  • Understand medical device regulations in the countries of the Middle East and North Africa
  • Understand What is a medical device and their classification
  • Clarify procedures for company and product registration
  • Discuss recent developments in the region
  • Opportunities to meet, network and share experiences with other industry colleagues

Who Should Attend:

This seminar will be of particular interest to:

  • Anyone involved in regulatory affairs for medical devices in the Middle East and North Africa
  • Anyone new to the region
  • Anyone interested in an update of recent developments

Agenda:

This course will cover Regulatory Activities in:
Algeria, Bahrain, Egypt, Israel, Iran, Iraq, Israel, Kuwait, Lebanon, Libya, Morocco, Oman, Palestine, Saudi Arabia, Sudan, Syria, Tunisia, UAE, Yemen & Jordan

Welcome and Introduction

The Medical Device Markets in the Middle East and North Africa

  • Markets and culture
  • Healthcare
  • Business culture
  • Economic overview
  • Regulatory environment and characteristics
  • General regulatory requirements
  • Company and product registration
  • Key documents needed
  • Basic structure of a dossier
  • Regulatory summary
  • Country presentations

Medical Devices and their Classification

  • What is a medical device
  • Different classes of products

Recent Developments in the Region

  • Harmonisation activities
  • Countries with new regulatory requirements for medical devices
  • Countries in the process of establishing regulatory guidance for obtaining marketing authorisations

Discussion will take place throughout the two days

For more information about this conference visit https://www.researchandmarkets.com/r/gcrr4f

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SOURCE Research and Markets