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Workshop on Clarifying the Regulatory Framework for Medical Devices and Supplies

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
Trade and Retail Council

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)

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