Health Products Regulation Group (HPRG) – Departmental Records Listing (1 January 2017 - 30 June 2017)

Page last updated: 16 August 2017

PDF version: Health Products Regulation Group (HPRG) – Departmental Records Listing (1 January 2017 - 30 June 2017) (PDF 68 KB)

File Number
FileTitle
HPRG - Health Products Regulation Group
E17-622 DRUG CONTROL ADMINISTRATION - Committees - Medicinal Cannabis Law Enforcement Working Group - Letter to Commissioners regarding establishment of a law enforcement single point of contact - Responses
E17-7558 DRUG CONTROL ADMINISTRATION - Legislation - Psychotropic Substances Act 1967 - Amendments
E17-6522 DRUG CONTROL ADMINISTRATION - Policy - Drug Regulation
E17-9979 DRUG CONTROL ADMINISTRATION - Policy - Hemp Seed in Food
E17-12054 GOVERNMENT RELATIONS - Legislation - Regulations to support 2016 Bill 1 measures
E17-1640 THERAPEUTIC GOODS REGULATION - Committees - Appointments - Specialist Advisors Completed Personal Details, Remuneration, TFN & Super Choice Forms
E17-260 THERAPEUTIC GOODS REGULATION - Committees - TGA Statutory Committees - Appointment / Reappointment 2017 paperwork
E17-3572 THERAPEUTIC GOODS REGULATION - Committees - TGA Statutory Committees and Specialist Advisors AGS Number
E17-14284 THERAPEUTIC GOODS REGULATION - Legislation - Changes to the Therapeutic Goods Act Advertising Legislation 2017-2018
E17-5690 THERAPEUTIC GOODS REGULATION - Legislation - Complementary Medicines - Medicines & Medical Devices Review (MMDR) - Legislative Development - MMDR Bill 2
E17-3359 THERAPEUTIC GOODS REGULATION - Legislation - Complementary Medicines Evaluation Section - CMES - 26BB Ingredient Updates
E17-3356 THERAPEUTIC GOODS REGULATION - Legislation - Complementary Medicines Evaluation Section - CMES - 26BB Legislative Alignment
E17-6268 THERAPEUTIC GOODS REGULATION - Legislation - Coordination of legislative changes for Review of Medicines & Medical Devices Regulation
E17-10133 THERAPEUTIC GOODS REGULATION - Legislation - Development of a new Therapeutic Goods Advertising Code 2017-2018
E17-590 THERAPEUTIC GOODS REGULATION - Legislation - Medicines Scheduling - Poisons Standard (SUSMP) - Update Feb 2018
E17-15189 THERAPEUTIC GOODS REGULATION - Legislation - Medicines Scheduling - Poisons Standard (SUSMP) - Update Jun 2018
E17-2315 THERAPEUTIC GOODS REGULATION - Legislation - Medicines Scheduling - Poisons Standard (SUSMP) - Update Mar 2017
E17-14050 THERAPEUTIC GOODS REGULATION - Legislation - SAS Category C Authorisations - Drafting of legislative instruments under Therapeutic Goods Act ss 19(7A) 32CM(7A) and 41HC(6)
E17-11048 THERAPEUTIC GOODS REGULATION - Policy - MMDIWG - Laccure vaginal pessary
E17-12358 THERAPEUTIC GOODS REGULATION - Policy - MMDR - Recommendation 24 and 26 - AP and SAS - Public consultation - Submissions for publication
E17-10682 THERAPEUTIC GOODS REGULATION - Policy - MMDR - Recommendations 24 & 25 - AP and SAS - Public Consultation - Submissions for publication
E17-3403 THERAPEUTIC GOODS REGULATION - Policy - MMDR - Recommendations 24 & 26 - AP and SAS - Public Consultation - Policy
E17-13063 THERAPEUTIC GOODS REGULATION - Policy - Procedure Packs with Custom Made Devices - 2017 Review
E17-6025 THERAPEUTIC GOODS REGULATION - Policy - Up-classification of surgical mesh
E17-4960 THERAPEUTIC GOODS REGULATION - Reviewing - Complementary Medicines - Regulatory Reforms - MMDR - Recommendation 35 & 36 (Ingredient Assessment) - Legislative changes
E17-4930 THERAPEUTIC GOODS REGULATION - Reviewing - Complementary Medicines - Regulatory Reforms - MMDR - Recommendation 38 (Permitted Indications) - Legislative changes
E17-4995 THERAPEUTIC GOODS REGULATION - Reviewing - Complementary Medicines - Regulatory Reforms - MMDR - Recommendation 42 (Variations) - Legislative changes
E17-5030 THERAPEUTIC GOODS REGULATION - Reviewing - Complementary Medicines - Regulatory Reforms - MMDR - Recommendation 47 (Appeal Rights) - Legislative changes
E17-6461 THERAPEUTIC GOODS REGULATION - Reviewing - Consultation: Review of the Scheduling Policy Framework and of advertising controls for Pharmacist-only medicines
E17-12807 THERAPEUTIC GOODS REGULATION - Reviewing - Review of the Scheduling Policy Framework S3 & of advertising controls for Pharmacist-only medicines