Workshop on Clarifying the Regulatory Framework for Medical Devices and Supplies - JCC
العربية
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- Jeddah Chamber
Jeddah Chamber
About the Chamber
Board of Directors
The Chamber's History
Work with Us
The City of Jeddah
About the Chamber
Board of Directors
The Chamber's History
Work with Us
The City of Jeddah
- Subscriber Services
Subscriber Services
Subscription Services
Approval Services
Commercial Services
Legal Services
Sectorial Councils’ Services
Saudi Business Boards
Commercial Delegation Services
Opportunities and Investment Ideas
Data Request Services
Partnerships and Suppliers Services
Advertising Services and Other Features
Subscription Services
Approval Services
Commercial Services
Legal Services
Sectorial Councils’ Services
Saudi Business Boards
Commercial Delegation Services
Opportunities and Investment Ideas
Data Request Services
Partnerships and Suppliers Services
Advertising Services and Other Features
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Programs and Initiatives
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Small and Medium Enterprises Support Center Programs
Community Development Center Programs
Small and Medium Enterprises Support Center Programs
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News and Events
News
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Exhibitions and Events
Basta Market - Season Seven
Jeddah Moves - Season 2
News
Workshops and Meetings
Exhibitions and Events
Basta Market - Season Seven
Jeddah Moves - Season 2
- Circulars and Publications
Circulars and Publications
Circulars
Publications
Reports and Information
Circulars
Publications
Reports and Information
- Added Value Projects
Added Value Projects
Warehouse City
Exhibition and Events Center
Jeddah International Business Center
Warehouse City
Exhibition and Events Center
Jeddah International Business Center
workshop
Workshop on Clarifying the Regulatory Framework for Medical Devices and Supplies
4/24/24
Goals
To explain the technical and regulatory requirements for medical devices and supplies
Axles
- Introduction to the legislative and regulatory framework for medical devices and supplies
- Specifications for the safety and performance of medical devices and supplies
- Requirements for obtaining marketing authorization for medical devices and supplies
- Requirements for safe use and post-market surveillance
- Innovation pathways and clinical studies
Speakers
- Eng. Abdulmohsen Al-Hajlan, Head of Post-Market Clinical Assessment Department
- Eng. Osama Al-Breikan, Senior Specifications and Regulations Expert
- Eng. Sahar Al-Malki, Senior Scientific Assessment Expert
- Eng. Samia Al-Oqaili, Senior Scientific Assessment Expert
- Eng. Abeer Al-Juhani, Product Registration Support Expert
Target Group
Medical device and supply companies, universities, research centers, and healthcare providers.
Organizer
Jeddah chamber
Participating Entities
Saudi Food and Drug Authority (SFDA)
Updates to the Contractor and Engineering Offices Classification System and Mechanism
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