Submissions
Medsafe Consultation: Guideline on the Regulation of Therapeutic Products in New Zealand: Clinical Trials
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Submission on the Therapeutic Products Act Repeal Bill
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SCOTT Terms of Reference Consultation Submission
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2023 Pharmacovigilance Guideline Consultation
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Pharmac Consultation: Paediatric cancer treatments in NZ
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Submission on the Therapeutic Products Bill
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Submission on Budget Policy Statement 2023
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Submission on Manatu Hauora LTIB Precision Health Consultation
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Medsafe Consultation: Proposed change to enable a labelling transition period when medicines are classified as a controlled drug or have a change to their controlled drug classification
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Submission to the Health Select Committee on the Medicines Amendment Bill (No 2)
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Submission to the Foreign Affairs, Defence and Trade Committee on the International treaty examination of the UK-NZ Free Trade Agreement
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Submission to the Education and Workforce Committee on the Accident Compensation (Maternal Birth Injury and Other Matters) Amendment Bill
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Medsafe Consultation: Proposed Revisions to CMN Form A
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Submission to the Pae Ora Legislation Committee on the Pae Ora (Healthy Futures) Bill
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PHARMAC Consultation: Proposal (dated 29 June 2021) to decline inactive funding applications
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Medsafe Consultation: Medsafe Fees Review
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PHARMAC Consultation: Revised Terms of Reference for CAC, PTAC and PTAC Sub-Committees and Associated PHARMAC Discussions document
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Medsafe Consultation: Plan to update the New Zealand Code of Good Manufacturing Practice
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PHARMAC Consultation: Proposal (dated 1 Oct 2020) to decline inactive funding applications 30 October 2020
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Medsafe Consultation: Revisions to Part 10 of the GRTPNZ
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PHARMAC Consultation: Proposal to widen access to adalimumab and award Principal Supply
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PHARMAC Consultation: Proposal to modify PHARMAC’s approach to competitive procurement
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Medsafe Consultation: Revisions to Part 8 of the GRTPNZ
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Medsafe Consultation: Proposed Warning Statement for Substances in Medicines
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Medsafe Consultation: Update to the Guideline on the Regulation of Therapeutic Products – Part 11: Clinical Trials
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Medsafe Consultation: Review of fees payable under the Medicines Regulation 1984
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Submission on international treaty examination of the comprehensive and progressive agreement for trans-pacific partnership (cptpp)
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Medsafe Consultation: Observers at Ministerial Advisory Committee meetings
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TGA submission on Nomenclature of Biological Medicines
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Response to the consultation document: PHARMAC's Implementation of the Trans-Pacific Partnership (TPP) provisions and other Amendments to Application processes
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Guideline on the Regulation of Therapeutic Products in New Zealand - Part 10: Requirements for information for prescribers and consumers (Edition 7.0)
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Submission to Foreign Affairs, Defence and Trade Select Committee on the Trans-Pacific Partnership Agreement (written & oral)
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Submission on Consultation Document: Implementation of the Trans-Pacific Partnership Intellectual Property Chapter
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Submission to foreign affairs, defence and trade select committee on the trans-pacific partnership agreement amendment bill
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Submission to foreign affairs, defence and trade select committee on the trans-pacific partnership agreement
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Submission on Update of the New Zealand Health Strategy Consultation Draft
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Response to Discussion Document Improving Access to Medicines and Devices in Primary Care
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Response to Pharmaceutical Margins
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Submission on Draft Code for Therapeutic and Health Advertising and Draft Guidance Notes
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Medsafe Consultation: Guideline on the Regulation of Therapeutic Products in New Zealand - Part 8: Pharmacovigilance (Edition 2.0)
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New Zealand Medicines and Medical Devices Recall Code
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PHARMAC Contestable Fund for Medicines for Rare Disorders Consultation and Draft RFP
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Joint Submission on PHARMAC OPP Decision Criteria Chaired by Medicines New Zealand
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Submission by Vaccines Member Companies of Medicines New Zealand to PHARMAC's Decision Criteria, Proposal for Change
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