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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)

To contact and inquire

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