Medical Device Regulations in the Middle East and North Africa

The size of the medical device market in the Middle East has expanded over recent years and this trend is forecast to continue. The growth is due in part to innovations in technology as the majority of Middle Eastern countries are early adopters of technological advancement, which provides opportunities for medical device companies. The regulatory environment in the region is also developing and this annual seminar will provide an essential overview of the key requirements for product approvals for medical devices in the Middle East and North Africa.

The programme will focus on the regulatory requirements and developments in individual countries and include interactive discussion sessions to allow you to exchange experiences with our expert faculty and other delegates.

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