Registration holders of currently registered products (including all veterinary medicines or agricultural chemical products that were registered at some time during the reporting period) are requested to provide the APVMA with an annual summary of all suspected adverse experiences, unless we request an interim report or more frequent reporting. The annual summary should be submitted using the forms below at the end of each financial year and no later than close of business on 30 September each year. A reminder notice is published in the APVMA Gazette each year.
PLEASE RETURN COMPLETED FORM TO:
Adverse Experience Reporting Program APVMA, PO Box 6182, KINGSTON ACT 2604
Phone:(02) 6210 4806
Fax:(02) 6210 4813
E-Mail: AERPcoordinator@apvma.gov.au
TEMPLATE - Refer Attachment
Registration holders of currently registered products (including all veterinary medicines or agricultural chemical products that were registered at some time during the reporting period) are requested to provide the APVMA with an annual summary of all suspected adverse experiences, unless we request an interim report or more frequent reporting. The annual summary should be submitted using the forms below at the end of each financial year and no later than close of business on 30 September each year. A reminder notice is published in the APVMA Gazette each year.
PLEASE RETURN COMPLETED FORM TO:
Adverse Experience Reporting Program APVMA, PO Box 6182, KINGSTON ACT 2604
Phone:(02) 6210 4806
Fax:(02) 6210 4813
E-Mail: AERPcoordinator@apvma.gov.au
TEMPLATE - Refer Attachment
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