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eatsafe.nzfsa.govt.nz ACVM Register New Zealand : Ministry for Primary Industries

Name of the Organization : Ministry for Primary Industries
Type of Facility : ACVM Register
Country : New Zealand

Website : https://eatsafe.nzfsa.govt.nz/web/guest

ACVM Register :

This register contains summary information on registered trade name products. It does not include provisional registrations or research approvals. This information is subject to change.

Related : Ministry for Primary Industries Afforestation Grant Scheme New Zealand : www.statusin.org/11212.html

For further information or detailed reports, email acvm-info@mpi.govt.nz Note that there may be a charge for specialised reports.

The products listed have been assessed to the ACVM Act registration information requirements and considered appropriate for registration. Conditions have been applied that are considered necessary and sufficient to manage the risks specified in section 4 of the ACVM Act 1997.

Some of the conditions on products impose prohibitions or obligations on persons other than the registrant (that is, importers, distributors, sellers or users). The label (information provided with the product) specifies any conditions imposed on users. It does not specify any conditions on importers, distributors, or sellers. These parties need to refer to this ACVM register for the conditions of registration for the product of interest.

Under the Agricultural Compound and Veterinary Medicines Act 1997 (ACVM Act) it is illegal for the registrant to manufacture, import, or sell a cancelled trade name product, from the date of its cancellation. For any other person, it is illegal to sell stock in trade or use a cancelled trade name product one year after the date of its cancellation. For example, if the date of cancellation stated is 20 March 2008 then it would be illegal to sell or use it after 20 March 2009.

Search Here : https://eatsafe.nzfsa.govt.nz/web/public/acvm-register

Conditions of registration:

Every veterinary medicine, agricultural chemical, or vertebrate toxic agent included in this register will have specific conditions from this list.

Retired conditions are not included in this list.

Condition 2:
The product must be manufactured in accordance with the ACVM Standard for Good Manufacturing Practice and to the chemistry and manufacturing specifications provided by the registrant and approved as part of the registration.

Condition 3:
Plant Compound: In addition to any labelling, advertising or promotion requirements specified in the current registration, labelling, advertising or promotion of the product must comply with the current ACVM – New Zealand Labelling and Advertising Guide for Plant Compounds Requiring Registration.

Condition 4:
The product must only be sold or imported according to the current registration.

Condition 6:
The product must not be used on any plant or in any manner specifically prohibited in the current registration.

Condition 8:
If the product is used on any food producing plant or on or around any plant not used to produce food:
** other than those specified on the current registration; or
** in a manner not specified in the current registration, the user must ensure that residues of any substance in the product that may occur in plant material produced from the plants treated, or in animal material produced from grazing or direct feeding of the plants treated to food producing animals, do not exceed the lesser of either:
** the specified residue limit in the current New Zealand (Maximum Residue of Agricultural Compounds) Food Standard and any subsequent amendments; or
** the default maximum residue limit in the current New Zealand (Maximum Residue of Agricultural Compounds) Food Standard and any subsequent amendments, when a maximum residue limit for that substance has not been specified.

Condition 11:
Veterinary Medicine: In addition to any labelling, advertising or promotion requirements specified in the current registration, labelling, advertising or promotion of the product must comply with the current ACVM – New Zealand Labelling and Advertising Guide for Veterinary Medicines Requiring Registration.

Condition 12:
The product may be used at the discretion of a registered veterinarian,
** when acting in accordance with any applicable code of practice approved under section 28 of the ACVM Act; and
** on animals under the direct care of that veterinarian, unless that use is specifically prohibited in the current registration.

Condition 14:
Class II Prescription Animal Remedy
The product must be sold only by an approved trader.

The product must be sold only to an approved trader, or to any person with a veterinary prescription or authorisation.

The product must be administered to an animal only by, in the presence of or under the control of a veterinarian, unless specified otherwise in the current approval.

Condition 15:
Class I Prescription Animal Remedy
The product must be sold only by an approved trader.

The product must be sold only to an approved trader, or to any person with a veterinary prescription or authorisation.

The product must be administered to an animal only by a veterinarian, or under and in accordance with the authority or prescription of a veterinarian.

Condition 16:
Over-the-counter Veterinary Medicine
The product may be sold or used by any person without a veterinary prescription.

The product must not be used by any person on animals or in a manner specifically prohibited in the current registration.

Use of the product by any person other than a veterinarian in any other animal or in any other manner other than those specified in the current registration must be done only after seeking veterinary advice.

Condition 17:
The product formulation and quantity must comply with and is limited to that specified in the application and Product Specific Approval.

Condition 19:
The conditions attached to the product must be given in writing and followed by any person involved in any aspect of the activities covered in the application.

Condition 20:
The product must only be used on the plants or animals specified and in the manner specified in the application and Product Specific Approval.

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