These forms are for the complementary medicines industry. For a complete list of forms, see: Forms

A C J L M N P R T

A

• Application for an Assessed listed medicine
  This application form is to be used to apply under section 23B of the Therapeutic Goods Act 1989 (the Act) to list a complementary medicine under section 16AE of the Act. This form is to be completed in conjunction with the Module 1.2.1: Assessed listed medicine general application form. Complete the form as per the instructions in the guidance for completing the application form for an assessed listed medicine.
• Assurances to accompany a L(A)1 application
  This form must be completed and submitted for all L(A)1 applications in Module 1.5.7 of the application. Completing this form provides the assurances required to accompany a L(A)1 application.
• Application for a new registered complementary medicine - grouped medicine
  Use to make an application for the registration of a new complementary medicine that would be subject to 'grouping' with a medicine already registered
• Application for evaluation of a new listed medicine substance
  This application form is used to apply under section 26BE of the Act to request that the TGA evaluates a new substance or change in requirements of an existing ingredient permitted for use in listed medicines. Complete the form as per the Evaluation of substances for use in listed medicines: application user guide.
• Australia-United States Free Trade Agreement
  The Australia-US Free Trade Agreement (the Agreement) came into force on 1 January 2005

C

• Compositional guideline template
  This template is for prospective sponsors and substance manufacturers to supply with their applications as described in the Australian Regulatory Guidelines for Complementary Medicines, Part 3, section 4.4
• Consent to supply goods that do not conform with subsection 9(2) of Therapeutic Goods Order No. 92 - Standard for labels of non-prescription medicines - section 14/14A

J

• Justification for a particular route of evaluation
  Use 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

L

• Listed medicines evidence package checklists
  These package checklists help sponsors and applicants of listed complementary medicines assess, record and present the available evidence for the indication/s for their medicine

M

• Module 1.2.1: Assessed listed medicine general application information form
  This form is to be completed in conjunction with the Assessed listed medicines application form. Complete the form as per the instructions in the guidance for completing the application form for an assessed listed medicine.

N

• Notification of a change in sponsorship
  Use to notify of a change in sponsorship of an ARTG entry
• Notification of a new proprietary ingredient
  Use to supply TGA with information about a proprietary ingredient
• Notification of an authorisation to use a protected ingredient form
  Use to authorise a sponsor to use a protected ingredient for the purpose of listing a medicine in the Register

P

• Pre-clearance application for animal-derived ingredients
  Assist users of the Electronic Listing Facility (ELF) seeking preclearance for animal derived ingredients by detailing what the TGA is looking for and what supporting documents need to be provided
• Proposal to amend the Required Advisory Statements for Medicine Labels (RASML)
  Use to propose an amendment to the Required Advisory Statements for Medicine Labels (RASML)
• Proposed 'Approved Herbal Name' (AHN) application form
  Use to propose a botanical name for a herb (an 'Approved Herbal Name' (AHN))
• Proposed Australian Approved Name (AAN) application form
  Use to apply for an Australian Approved Name
• Proposed Australian Biological Name (ABN) application form
  Use to apply for an Australian Biological Name.
• Proposed 'Herbal Substance Name' (AHS) application form
  Use to apply for a name for a herbal material that is fully characterised in a monograph or pharmacopoeia (a 'Herbal Substance Name' (AHS)).

R

• Registered medicine variation form (complementary medicines)
  Use to vary the particulars of complementary medicines which are already registered in the ARTG
• Request to cancel an entry/entries from the Australian Register of Therapeutic Goods (ARTG)
  Use to cancel an entry from the ARTG

T

• TGA Business Services forms
  Forms for sponsors, agents and manufacturers to apply for access to TGA Business Services