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Use this form when submitting an updated RMP after regulatory approval. This form should be submitted in module 1.0.1 and the updated RMP in module 1.8.2.
Submit your updated RMP/ASA as a NeeS/eCTD sequence.
See 'Risk management plans for medicines and biologicals: Australian requirements and recommendations' for information about when to submit updated RMPs.
Submission of an updated RMP
These forms are available in pdf and Microsoft Word formats. The pdf form can be filled in and saved to your computer using Adobe Reader version 7 or later or any version of Adobe Acrobat Standard or Professional. If you have an earlier version of Adobe Reader you can fill in the form on-screen and print it out but you will not be able to save the completed form.