Submissions on the Natural Health Products Regulations and Notices closed on Friday 4 March. However, submissions on the Draft list of conditions about which a claim can be made and the Draft database of permitted substances remains open until 31 October 2016.
How to have your say
The Ministry welcomes all feedback. The formal consultation period for the Regulations and Notices has now closed, but there are two components you can still give feedback on, namely the draft list of permitted substances and the draft list of conditions about which a claim can be made.
Please get in touch with us by emailing firstname.lastname@example.org
or by posting your submission to
Natural Health Products
Ministry of Health
PO Box 5013
All submissions on the two lists are due by 31 October 2016 at 5pm.
After commencement of the legislation a formal process will be established for submission on these lists and there will be a fee charged for this service.
The Government is developing a new regulatory scheme for low-risk natural health products, and is interested in public feedback on the proposals outlined in the consultation document and the draft papers:
- The Regulation of Natural Health Products: Consultation document (docx, 364 KB)
- The Regulation of Natural Health Products: Consultation document (pdf, 135 KB)
- Draft Code of Manufacturing Practice (docx, 199 KB)
- Draft Code of Manufacturing Practice Guidelines (docx, 275 KB)
- Draft Guidelines for Natural Health Products Evidence Requirements (docx, 135 KB)
- Draft list of conditions about which claims can be made (xlsx, 32 KB)
- Draft database of permitted substances
Your feedback is important because it will help shape the final proposals in the regulations, ensuring they are workable and that the purpose of the legislation is achieved. We appreciate you taking the time to make a submission.
In particular, your feedback is sought on:
- what the regulations and notices will specify
- labelling requirements
- fees associated with manufacturing and selling permitted NHPs
- type and quality of evidence used to support health benefit claims
- manufacturing requirements
- permitted substances
- conditions about which claims can be made.
The Bill is expected to take effect around June 2016, and the Regulations are expected to come into force shortly afterwards.