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Guideline on quality of oral modified release products
[PDF, 180.85 KB]
About this guideline
Overseas effective date: 6 months after publication (published 20 March 2014)
Replaces: CPMP/QWP/604/96 Note for Guidance on Quality of Modified Release Products: [A: Oral Dosage Forms] (adopted by TGA 19 April 2001)
Categories: Quality | Specific types of products
TGA annotations:
EU-specific procedural requirements stated in this Guideline do not apply in Australia.
- Where EU guidelines adopted in Australia include references to EU legislation (including EC Directives and Regulations), the requirements contained in the referenced EU legislation are not applicable to the evaluation of medicines by the TGA.
- All documents and other content published by the European Medicines Agency (EMA) on this website are under the copyright and other intellectual property rights ownership of the EMA. Please refer to Legal notice | European Medicines Agency for further information.
For more information see International scientific guidelines adopted in Australia.