Dublin, Jan. 31, 2024 (GLOBE NEWSWIRE) -- The "Medical Device Regulations in the Middle East and North Africa Training Course" conference has been added to ResearchAndMarkets.com's offering.
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.
Benefits of attending:
- 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
Certifications:
- CPD: 12 hours for your records
- Certificate of completion
The event 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
The medical device markets in the Middle East and North Africa (MENA):
- 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
Medical Devices and their classification:
- What is a medical device
- Different classes of products
Individual Country Presentations:
Algeria, Bahrain, Egypt, Israel, Iran, Iraq, Jordan, Kuwait, Lebanon, Libya, Morocco, Oman, Palestine, Saudi Arabia, Sudan, Syria, Tunisia, UAE and Yemen
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
Economic Overview:
- Saudi Arabia
- GHC/Prequalification GPP
- Bahrain
- Qatar
- Oman
- Yemen
- Kuwait
- UAE
- Egypt
- Sudan
- Algeria
- Morocco
- Tunisia
- Israel
- Palestine
- Syria
- Jordan
- Lebanon
- Iraq
- Iran
Medical Device Network
Discussion sessions will take place throughout the two days
For more information about this conference visit https://www.researchandmarkets.com/r/oxpsct
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