A-Z guide
A B C D E F G H I L M N O P R S T W
A
- Adverse Drug Reactions Advisory Committee (ADRAC)
- Advertising medicines to consumers
- Advertising prescription medicines to health professionals
- Advertising therapeutic goods
- Advisory Committee on Biologicals (ACB)
- Advisory Committee on Complementary Medicines (ACCM)
- Advisory Committee on Medical Devices (ACMD)
- Advisory Committee on Non-prescription Medicines (ACNM)
- Advisory Committee on Prescription Medicines (ACPM)
- Advisory Committee on the Safety of Medical Devices (ACSMD)
- Advisory Committee on the Safety of Medicines (ACSOM)
- Advisory Committee on the Safety of Vaccines (ACSOV)
- Advisory committees on medicines & chemicals scheduling (ACMS & ACCS)
- Alerts
- Australia New Zealand Therapeutic Products Agency (ANZTPA)
- Australian Adverse Drug Reactions Bulletin
- Australian code of good manufacturing practice for human blood and blood components, human tissues and human cellular therapy products
- Australian code of good wholesaling practice for medicines in schedules 2, 3, 4 & 8
- Australian Drug Evaluation Committee (ADEC)
- Australian Influenza Vaccine Committee (AIVC)
- Australian pharmacovigilance requirements and recommendations for medicine sponsors
- Australian Public Assessment Reports for prescription medicines (AusPARs)
- Australian Register of Therapeutic Goods
- Australian regulation of over-the-counter medicines
- Australian regulation of prescription medical products
- Australian regulatory guidelines for biologicals (ARGB)
- Australian regulatory guidelines for complementary medicines (ARGCM)
- Australian regulatory guidelines for medical devices (ARGMD)
- Australian regulatory guidelines for OTC medicines (ARGOM)
- Australian regulatory guidelines for prescription medicines (ARGPM)
- Australia-United States Free Trade Agreement
- Authorised prescribers
B
- Black salve, red salve and cansema
- Blood, tissues & biologicals
- Buying medicines and medical devices over the Internet
- Report of lymphoma associated with breast implants
C
- Cancellations from the ARTG following compliance review
- Capability map
- Clinical trials
- Colloidal silver & related products
- Colourings permitted in medicines for oral use
- Committees
- Common technical document (CTD)
- Complementary medicines
- Complementary Medicines Evaluation Committee (CMEC)
- Compliance with ministerial and default standards
- Compositional guidelines
- Consultations & reviews
- Consumer guide to commonly noted advertising breaches
- Consumer Medicines Information (CMI)
- Contact the TGA
- Copyright
- Cosmetics
- Counterfeit medicines and devices
D
E
- Electronic cigarettes
- Employment & job vacancies
- European Union guidelines
- Events, training & presentations
- Excluded goods orders
- Exporting blood, tissues & biologicals
- Exporting medical devices
- Exporting medicines
F
G
- Good manufacturing practice - an overview
- Groups orders
- Guidance for industry on electronic prescription medicine submission dossiers
- Guidelines for levels and kinds of evidence to support indications and claims
H
- Health Technology Assessment (HTA)
- Herbal materials & extracts
- How the TGA regulates
- How therapeutic goods are regulated in Australia
- Human Research Ethics Committees and the therapeutic goods legislation
I
- Import & export
- In vitro fertilisation (IVF) solutions
- Ingredients/excipients in Listed medicines
- International
- International Medical Device Regulators Forum (IMDRF)
- International Regulators Consortium
- IVD guidance documents
L
- Labelling & packaging
- Labelling and packaging review
- Legislation & legislative instruments
- Listing notices
- Literature-based submissions - points to consider
M
- Manufacturer statutory declarations
- Manufacturing principles & guidelines
- Manufacturing principles for medicinal products
- Manufacturing therapeutic goods
- Media releases & statements
- Medical device incident reporting & investigation scheme (IRIS)
- Medical device incident reporting & investigation scheme (IRIS) articles
- Medical devices & IVDs
- Medical Devices Evaluation Committee (MDEC)
- Medical devices notices & standards orders
- Medical Devices Vigilance and Monitoring (MDVM) email list for Australian health professionals
- Medicines and TGA classifications
- Medicines Evaluation Committee (MEC)
- Medicines Safety Update
- Medicines Safety Update email list
N
- Nanotechnology and therapeutic products
- National Coordinating Committee on Therapeutic Goods (NCCTG)
- National Drugs and Poisons Schedule Committee (NDPSC)
- News & public notices
O
- Orders that goods are therapeutic goods
- Orphan drugs
- Other therapeutic goods
- Over-the-counter medicines
P
- Personal Importation Scheme - bringing unapproved medicines or medical devices into Australia by mail, courier or in person
- Pharmacopoeias
- Poly Implant Prothese (PIP) breast implants - the Australian perspective
- Prescribing medicines in pregnancy database
- Prescription medicines
- Price information code of practice
- Product Information (PI)
- Product recalls
- Publications
R
- Recall of DePuy Orthopaedics ASR hip replacement device
- Regulatory affairs consultants
- Regulatory and Technical Consultative Forum for medical devices (RegTech Forum)
- Reporting problems
- Required advisory statements for medicine labels (RASML)
- Restricted representations
- Risk management plans for prescription medicines
- RSS feeds
S
- Schedule 1 certificates
- Schedule 1 of the Therapeutic Goods Regulations explained
- Schedule 3 advertising guidelines
- Scheduling of medicines & poisons
- Section 23 instruments
- Section 7 declarations - food or therapeutic good?
- Single therapeutic goods orders
- Site master file preparation: PIC/S explanatory notes for pharmaceutical manufacturers
- SMP email list
- Special access scheme
- Standards orders and medical devices
- Streamlined submission process for prescription medicines
- Subscribe to updates
- Sunscreen standard 2012: information for industry
- Sunscreen standard 2012: information for retailers
- Sunscreens
- Sunscreens: information for consumers
T
- Tamper-evident packaging code of practice
- Tampons & menstrual cups
- TGA approved terminology for medicines
- TGA AusPAR email list
- TGA Consultations email list
- TGA Safety Information email list
- TGA Update email list
- The Poisons Standard (the SUSMP)
- Therapeutic Device Evaluation Committee (TDEC)
- Therapeutic goods advertising code
- Therapeutic Goods Committee (TGC)
- Therapeutic goods determinations
- Therapeutic goods information specifications
- Therapeutic goods orders
W
Web page last updated: Thursday, 3 February 2011
URL: http://www.tga.gov.au/about/website-azguide.htm