Form: Consultation: Alignment with European medical device regulatory framework
This form is used to accompany a submission made on this TGA consultation.
This form, when completed, will be classified 'For official use only'.
For guidance on how your information will be treated by the TGA see: Treatment of information provided to the TGA.
For more information about the Australian Privacy Principles, visit the Office of the Australian Information Commissioner's website.
Service Provided By
Therapeutic Goods Administration - Department of Health