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Health Sciences Authority
Regulatory Updates

Good Submission Practice Workshop

Audiences

Industry member

Product type

Medical devices

12 September 2024

This article has been migrated from an earlier version of the site and may display formatting inconsistencies.

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 [PDF, 2162 KB]

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