Workshop on Clarifying the Regulatory Framework for Medical Devices and Supplies - JCC
workshop
Workshop on Clarifying the Regulatory Framework for Medical Devices and Supplies
4/24/24
Date
10:00am - 1:00pm
Locaton
Jeddah Chamber - Juffali Hall, First Floor
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)
مقدمة لآليات المحتوى المحلي للجهات الحكومية
مبنى غرفة جدة الرئيسي - قاعة الجفالي - الدور الاول
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