Presented by TÜV SÜD Malaysia and global experts, our webinars provide you with information on the latest regulations and standards that affect industries, giving you practical advice on how to ensure your operations comply to current and future safety, quality and environmental requirements and legislation.
We provide both live and on-demand webinars providing you with the opportunity to interact and quiz our experts, or to have the convenience of watching the webinar at a time that suits you.
Our expert will provide a comprehensive understanding on the requirements and key elements pertaining to the biological evaluation of medical devices.
The Packaging module under MDR captures a holistic insight on the expectations by the Notified Body, in order to understand the documentation for the usability evaluation of the sterile barrier system.
The Sterilization module under MDR covers a comprehensive discussion about EO residuals, in relation to patient population.
This module aims to provide a holistic understanding on the Technical Documentation Assessment according to Annex IX Chapter II.
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Bosnia and Herzegovina