This consultation closes on 3 February 2020
The TGA sought comments from interested parties on an update to guidance for:
- Export of medicines from Australia
- Export certification for medical devices
On this page: Consultation documents | Consultation questions | Timetable | About the consultation | Content of submissions | What will happen | Privacy information | Enquiries
How to access a pdf or Word document
Export of medicines from Australia
- Consultation: DRAFT Export of medicines from Australia (pdf,330kb)
- Consultation: DRAFT Export of medicines from Australia (docx,102kb)
Export certification for medical devices
- Consultation: DRAFT Export certification for medical devices (pdf,201kb)
- Consultation: DRAFT Export certification for medical devices (docx,97kb)
We invited feedback regarding the following proposals:
- Is it of benefit to allow submission of electronic schedules to accompany a Certificate of Pharmaceutical Product (CPP) or a Certificate of Listed Product (CLP) application?
- we currently require all export documents to be provided in hard copy to the TGA, as this was a requirement of importing countries over 15 years ago
- we would like to allow the option to submit electronic documents (where acceptable to the importing country)
- Is it of benefit for the TGA to provide traceable post for all hard copy certificates?
- this may incur an appropriate fee increase
Document released for consultation on Monday, 9 December 2019
Interested parties should respond by close of business Monday, 3 February 2020.
Feedback will be released following consideration of submissions. (See 'What will happen').
About the consultation
To export therapeutic goods from Australia, certain regulatory requirements set out in Australia's therapeutic goods legislation in addition to other relevant Commonwealth and state or territory legislation must be met. The Therapeutic Goods Administration (TGA) is responsible for administering the therapeutic goods legislation.
This updated guidance provides clarification of TGA export policy.
Content of submissions
Submissions may address any, or all, of the guidance content, proposals or identified issues.
Any questions relating to submissions should be directed to the Prescription Medicines Authorisation Branch, by email to email@example.com.
What will happen
All submissions will be placed on the TGA Internet site unless marked confidential or indicated otherwise in the submission cover sheet (see Privacy information).
Submissions will be reviewed by the TGA and feedback on submissions will be provided through this website.
Once finalised, the updated guidance will be published on the TGA website.
- The TGA collects your personal information in this submission in order to:
- contact you if the TGA wants to seek clarification of issues raised in your submission or to check whether you consent to certain information that you have provided being made publicly available.
- help provide context about your submission (e.g. to determine whether you are an individual or a director of a company or representing an interest group).
- seek feedback about how the consultation was undertaken.
- Please do not include personal information about other individuals in the body of your submission. Personal information in this context means information or an opinion about an individual whose identity is apparent, or can reasonably be ascertained, from the information or opinion.
- More information on consultations and privacy is included in the submission form and on our website.