Workshop

Beneficiaries

All

Individual

Investor

Health practitioners

Objectives: •  To know about additional Risk Minimization Measures (aRMMs) and the SFDA role. •  To Lear ...

2022-12-19 - 2022-12-19

Brief: Explain the Requirements for conduct clinical trials in Saudi Arabia according to ISO 14155   Work ...

2022-12-14 - 2022-12-14

» Objectives   During this workshop all relevant aspects regarding the quality assessment of post approval changes ...

2022-11-21 - 2022-11-21

Brief: Overview of UDI requirements  The Required data for submission Advice & recommendations & ...

2022-11-16 - 2022-11-16

Brief: Explaining the risk management file (RMF) for medical devices and the compliance with the requirements of ISO ...

2022-11-01 - 2022-11-01

Brief: Explain the main content of the Requirments for Biological Evaulation and Biocompatibility of Medical Devices ...

2022-10-26 - 2022-10-26

Brief: Requirements of Clinical evaluation report and post market clinical follow-up,  explanation of the conten ...

2022-10-25 - 2022-10-25

Brief:    •  An overview of verification and validation section requirements      ...

2022-10-24 - 2022-10-24

Brief: In this workshop, attendance will learn the following points regarding the new service of “Overseas Medical De ...

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