ACMPR
Marijuana for Medical Purposes
JOHN SIMON AND ASSOCIATES LTD.
Licensed producers will be required to meet all the requirements of the Access to Cannabis for Medical Purposes Regulations (ACMPR) including, but not limited to:
- Physical Security Measures
- Good Production Practices
- Packaging, Labelling and Shipping Requirements
- Import and Export permit, if applicable
- Security Clearance
The following excerpt from the guidance document to help licensed producers understand the requirements under the ACMPR. It is the responsibility of the licensed producer to understand the ACMPR and to be knowledgeable about their obligations.
SECTION 10 FOR THE APPLICATION FORM: QUALITY ASSURANCE PRE-LICENSING REPORT
- As per paragraph 23(4)(h) of the MMPR, a document, signed and dated by the proposed quality assurance person required in section 60 of the MMPR, must be included that details the quality assurance person’s qualifications and etablishes that the buildings, equipment and sanitation program comply with the requirements of Division4. Please ensure that the quality assurance person signs and dates this document to complete this portion of the application.
- As per subparagraph 23(4)(h)(ii) of the MMPR, you re required to submit a complete Quality Assurance report establishing that the buiding(s), equipment and sanitation program comply with the requirements of Division 4. You must include a description in your Quality Assurance report that the building(s), equipment and sanitation program used at your site will be in compliance with sections 55, 56 and 57 of Division 4 of the MMPR.
- For more information on quality assurance compliance and what must be included in your Quality Assurance Pre-Licensing Report please refer to Division 4 (sections 52-63) of the MMPR and the Technical Specifications for Testing Dried Marihuana for Medical Purposes guidance document found online at http://www.hc-sc.gc.ca/dhp-mps/marihuana/info/add-supp-eng.php.