Forms for sponsors of prescription medicines
Prescription medicines forms
- Prescription medicine registration form & guide
<http://www.tga.gov.au/docs/html/pmrvform.htm>
Use to apply for registration or to vary the conditions of registration for prescription medicines in Australia - Supply of information for the creation of a Provisional ARTG Record (PAR)
<http://www.tga.gov.au/docs/html/forms/parform.htm>
Use to apply to the Drug Safety and Evaluation Branch for the creation of a provisional ARTG record - Summary of a bioavailability or bioequivalence study
<http://www.tga.gov.au/docs/html/forms/pmbiosum.htm>
Use to submit a summary of a bioavailability or bioequivalence study - Notification of proposal to submit supplementary data and submission of supplementary data
<http://www.tga.gov.au/docs/html/forms/suppdata.htm>
Use to notify the TGA of a proposal to submit supplementary data and to submit supplementary data - Report of the manufacture of exempt therapeutic goods
<http://www.tga.gov.au/docs/html/forms/exempttg.htm>
Used by sponsors of exempt therapeutic goods to inform the TGA of the details of the supply of such goods on a quarterly basis - Therapeutic goods and use of human embryos or human embryonic stem cells or material derived therefrom
<http://www.tga.gov.au/docs/html/forms/stemcell.htm>
Use this form for products that are manufactured using a human embryo or a human embryonic stem cell, or any material sourced from a human embryo or human embryonic stem cell - Justification for a particular route of evaluation
<http://www.tga.gov.au/docs/html/forms/justsch10.htm>
To be completed when an applicant wishes to have their product or substance evaluated by an area of the TGA other than as specified in Schedule 10 to the Therapeutic Goods Regulations - Notification of a proprietary ingredient
<http://www.tga.gov.au/docs/html/forms/notifpi.htm>
Allows proprietary ingredient formulations to be entered onto the ARTG
Related (general) forms
- Client details form
<http://www.tga.gov.au/docs/html/forms/clientdt.htm>
To be completed by or for each client involved with the supply of the therapeutic goods in Australia for which the TGA requires address details - Australia-US Free Trade Agreement certificates
<http://www.tga.gov.au/international/usfta.htm>
The Australia-US Free Trade Agreement came into force on 1 January 2005 - Authorisation to cancel a product from the Australian Register of Therapeutic Goods
<http://www.tga.gov.au/docs/html/forms/artg-cancel.htm>
Use to request cancellation of the registration/listing/inclusion of medicines and/or devices on the ARTG - Request to transfer the sponsorship of an ARTG entry - relinquishing company
<http://www.tga.gov.au/meds/tsfrelinqco.htm>
Used by the relinquishing company to request to transfer the sponsorship of an ARTG entry - Request to transfer the sponsorship of an ARTG entry - accepting company
<http://www.tga.gov.au/meds/tsfacceptco.htm>
Used by the accepting company to request to transfer the sponsorship of an ARTG entry
