TGA Webinar: Preparing a product information document for a generic medicine – quality and regulatory expectations

The TGA is holding a webinar on Wednesday 5 June 2024, 2:00-3:00pm AEST, which aims to provide information on the TGA’s expectations regarding the quality aspects of a Product Information document for generic medicines and to clarify most common deficiencies and answer frequently asked questions.

The webinar may be of interest to applicants of Registered Complementary Medicines (RCM) for restricted RCM medicines (such as Schedule 3 medicines), Category 4 (RCM 4) or Category 5 (RCM 5 ) applications.

Register for the webinar here.

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