Microsoft word - wd-lic-4 2-1.docx

Application for a Licence to Deal in Controlled Drugs
F
Forward completed application to:
Medicines Control, PO Box 5013, WELLINGTON 6145
Pursuant to regulation 3 of the Misuse of Drugs Regulations 1977, I hereby apply for a Licence
to Deal in the Controlled Drugs indicated on
OR
Name and postal address of body
Name and postal address of individual
corporate:
applicant:

Street address of applicant’s premises to which the licence is to apply:

__________________________________________________ __________________________________________________
Distributor’s

s name and address (if other than applicant):
__________________________________________________ _________________________________________
The licence is required to allow controlled drugs to be:


For Manufacture: Please provide the names, strengths and quantities of controlled drugs to be
manufactured during the proposed licensing period (on a separate sheet iif required)
__
__________________________________________________ __________________________________________________ __________________________________________________ __________________________________________________
Nature of business and if supply is included, who the controlled drugs are to be supplied
to:
__
__________________________________________________ __________________________________________________ Application for a Licence to Deal in Controlled Drugs v2.1 Medicines Control, Provider Regulation RESPONSIBLE PERSONS

Details of persons nominated to be responsible persons:
Name

APPLICANT DETAILS

Current/previous licence number: _____________ Expiry Date: _____________
(if applicable)

Name:
____________________________________
Job title: __________________________________

Telephone number:
_________________________

Fax number:
_______________________________

Email:
____________________________________

Signature:
_____________________________ Date: __________________________

Application for a Licence to Deal in Controlled Drugs v2.1 Medicines Control, Provider Regulation Schedule to Application for Licence to Deal in Controlled Drugs

CONTROLLED DRUGS APPLICANT PROPOSES TO DEAL IN:-
Class B, Part I
 gamma hydroxybutyrate (GHB)  morphine hydrochloride  tetrahydrocannabinols (THC) (except when contained in a Class C controlled drug)  2-methylamino-1-(3,4methylenedioxyphenyl) propane (MDMA) Class B, Part II
 methylphenidate hydrochloride  ephedrine Class B, Part III
Class C, Part I
Class C, Part II
 dextropropoxyphene napsylate/hydrochloride (not being a Class C, Part V drug) Class C, Part III
Class C, Part IV
Class C, Part V
 dextropropoxyphene preparations (as described in Class C, Part V) Other controlled drugs not listed above: ________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________ Application for a Licence to Deal in Controlled Drugs v2.1 Medicines Control, Provider Regulation
Appendix I

Applications from Research, Testing and Teaching Organisations

Physical address where CD safe is located:
Building No.
Department
Teaching
Institution

Name of the Code of Practice the institution works under:
___________________________________________________________________

How are the medicines and/or controlled drugs to be used?
___________________________________________________________________
___________________________________________________________________
___________________________________________________________________

Where are the medicines and/or controlled drugs purchased from?
___________________________________________________________________

Does the applicant import controlled drugs?


If yes, does the applicant obtain import
permits?

What form of recordkeeping is kept on site? i.e. controlled drug register

___________________________________________________________________

If live animals are involved, what is the name of the veterinarian in charge or to
whom the responsible persons work under the direction of?
___________________________________________________________________
Application for a Licence to Deal in Controlled Drugs vDRAFT2.1 Medicines Control, Provider Regulation

Source: http://www.alcp.org.nz/docs/application_deal.pdf

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