Medical Device Regulations in the Middle East and North Africa Region
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 such as Algeria, Bahrain, Egypt, Iran, Iraq, Jordan, Kuwait, Lebanon, Libya, Morocco, Oman, Palestine, Saudi Arabia, Sudan, Syria, Tunisia, UAE, and Yemen.Gain an introduction to the medical device markets: countries, numbers, economic facts, and trends, the regulatory environmentUnderstand medical device regulations in the MENA regionGet an overview of registration requirements, timelines, feesClarify procedures for company and product registrationMedical Device regulations is an evolving era in the MENA region. Most of the MENA governments have published regulatory guidance as registration for some devices is required for importation.Areas CoveredOverview of the key areas of registration requirements for product and company approvals for medical devices in the Middle East and North Africa.Course Level - Basic/IntermediateWho Should AttendAnyone involved in regulatory affairs for medical devices in the MENA regionAnyone new to the regionAnyone interested in an update of recent developmentsWhy Should You Attend To understand the registration requirements for medical devices in the key markets in the MENA region to be able to efficiently plan submission strategies for the region.
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Industries
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Life Sciences
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Medical Devices
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Webinars
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Live Webinar
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On-Demand Webinar
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 such as Algeria, Bahrain, Egypt, Iran, Iraq, Jordan, Kuwait, Lebanon, Libya, Morocco, Oman, Palestine, Saudi Arabia, Sudan, Syria, Tunisia, UAE, and Yemen.
- Gain an introduction to the medical device markets: countries, numbers, economic facts, and trends, the regulatory environment
- Understand medical device regulations in the MENA region
- Get an overview of registration requirements, timelines, fees
- Clarify procedures for company and product registration
Medical Device regulations is an evolving era in the MENA region. Most of the MENA governments have published regulatory guidance as registration for some devices is required for importation.
Areas Covered
Overview of the key areas of registration requirements for product and company approvals for medical devices in the Middle East and North Africa.
Course Level - Basic/Intermediate
Who Should Attend
- Anyone involved in regulatory affairs for medical devices in the MENA region
- Anyone new to the region
- Anyone interested in an update of recent developments
Why Should You Attend
To understand the registration requirements for medical devices in the key markets in the MENA region to be able to efficiently plan submission strategies for the region.