Good Submission Practice Workshop
The Medical Devices Cluster (MDC) conducted a Good Submission Practice Workshop on Wednesday, 28 August 2024. The primary objective of this workshop was to emphasize the critical documentary requirements often overlooked during submissions. This aimed to empower stakeholders to furnish good submission documents, thereby ensuring expedited processing or resolution of their applications. The scope of submissions encompasses Product Registration, Change Notification, Field Safety Corrective Action (FSCA), Adverse Events and Dealer's Licence.
For more information, please refer to the presentation slides below:
Good Submission Practice 2024
Industry member, Medical devices
Published:
Regulatory Updates