You must comply with regulatory requirements when making, supplying, or distributing registered complementary medicines.
Registered complementary medicines must be manufactured in accordance with legislated Good Manufacturing Practice (GMP) standards to ensure their quality, safety and efficacy.
You are responsible for maintaining quality during production, supply, transport, and distribution.
We regulate these activities to protect public health and ensure registered complementary medicines remain safe and effective.
If you import or export registered complementary medicines, you must comply with Australian laws.
You must meet certain obligations to legally supply therapeutic goods in Australia. This section contains guidance and information specific to registered complementary medicines. You may also have to meet obligations that apply to all medicines and all products.
Good Manufacturing Practice
Understand the standards for Good Manufacturing Practice.
-
GuidanceGuidance for interpreting the Pharmaceutical Inspection Co-operation Scheme (PIC/S) guide to good manufacturing practice (GMP) for medicinal products.
-
GuidanceGuidance for interpreting the Pharmaceutical Inspection Co-operation Scheme (PIC/S) guide to good manufacturing practice (GMP) for medicinal products.
-
PageComplying with the Pharmaceutical Inspection Co-operation Scheme (PIC/S) guide to Good Manufacturing Practice (GMP).
-
-
PageGood Manufacturing Practice (GMP) describes a set of principles and procedures that when followed helps ensure that therapeutic goods are of high quality.
-
GuidanceThis guidance explains good manufacturing practice (GMP) requirements for Australian sponsors and manufacturers of medicines, active pharmaceutical ingredients (APIs) and sunscreens.
-
PageRegulatory responsibilities and expectations for medicine manufacturers.
-
GuidanceGuidance for interpreting the Pharmaceutical Inspection Co-operation Scheme (PIC/S) guide to good manufacturing practice (GMP) for medicinal products.
-
GuidanceGuidance for interpreting the Pharmaceutical Inspection Co-operation Scheme (PIC/S) guide to good manufacturing practice (GMP) for medicinal products.
-
GuidanceGuidance for interpreting the Pharmaceutical Inspection Co-operation Scheme (PIC/S) guide to good manufacturing practice (GMP) for medicinal products.
-
PageUnderstand your record keeping responsibilities.
-
GuidanceGuidance for interpreting the Pharmaceutical Inspection Co-operation Scheme (PIC/S) guide to good manufacturing practice (GMP) for medicinal products.
-
PageRegulatory requirements, principles, standards and record keeping apply to manufacturers of medicines and biologicals.
-
GuidanceGuidance for interpreting the Pharmaceutical Inspection Co-operation Scheme (PIC/S) guide to good manufacturing practice (GMP) for medicinal products.
-
GuidanceGuidance on good manufacturing practice (GMP) compliance requirements for domestic and overseas manufacturers of medicines and biologicals.
GMP clearance
Access information on applying for GMP clearance.
-
Decision treeUse the GMP Clearance Application Assistance Tool (CAAT) to assist in determining the general evidence requirements for your GMP clearance applications.
-
PageSearch the Code Tables for codes needed to apply for good manufacturing practice (GMP) clearance.
-
User guideThis user guide is for sponsors wanting to submit GMP clearance application by the TGA Business services (TBS) portal.
-
User guideCheck out our user guide to assist sponsors when using the code tables for GMP Clearance applications.
-
PageInformation about current processing times, workload, priorities, and key messages for GMP Clearance applications.
-
PageFind out about obtaining Good Manufacturing Practice (GMP) clearance for an overseas manufacturing site.
-
PageThis information explains your responsibilities when obtaining Good Manufacturing Practice (GMP) clearance by any pathway, or by GMP certification following our inspection.
Licensing
Find out how to apply for, vary or maintain a manufacturing licence.
-
PageThere is an annual charge for the manufacturing of therapeutic goods.
-
User guideA step-by-step guide for Australian manufacturers of therapeutic goods.
-
Decision treeUse this decision tree to assist you to determine if GMP licencing or certification is required.
-
PageA step-by-step guide for Australian manufacturers of therapeutic goods (other than medical devices) applying to vary a manufacturing licence.
-
PageRevocation of manufacturing licence due to non-payment.
-
PageAs part of the revised GMP fees and charges, this information has been updated to reflect changes in TBS.
-
PageThis guidance is for Australian manufacturers who wish to transfer a manufacturing licence to another entity.
-
PageVary your Good Manufacturing Practice (GMP) clearance or licence.
Certification
Access information on applying for or varying certification.
-
User guideA step-by-step guide for Australian manufacturers of therapeutic goods.
-
PageThis information is for Australian sponsors or agents of Australian sponsors of overseas manufacturers making GMP certification applications.
-
PageThis information explains your responsibilities when obtaining Good Manufacturing Practice (GMP) clearance by any pathway, or by GMP certification following our inspection.
Inspections
Learn how TGA conducts inspections of manufacturing sites.
-
PageWhen we inspect a manufacturer for compliance with GMP, we assess your level of compliance with the manufacturing principles and any other requirements (such as TGOs and conditions of authorisation)
-
PageWe regularly inspect manufacturers of medicines and biologicals, using a risk-based approach, to ensure compliance with manufacturing principles.
-
PageA manufacturer's compliance level is determined by the number and nature of deficiencies found during inspections, and their response to the inspection report.
-
PageManufacturers of therapeutic goods are regularly inspected to ensure compliance with manufacturing principles.
-
-
PageWe employ a risk-based approach to the frequency of manufacturer inspections.
-
PageManufacturer inspections and their frequency are guided by the inherent risks of a product.
-
PageManufacturers of therapeutic goods are regularly inspected by the TGA using a risk-based approach to ensure compliance with GMP standards.
-
PageAll timeframes are variable depending on the cooperation of manufacturers, sponsors and sometimes international regulatory agencies
Product types