I currently have two LP's waiting for inspections that were scheduled by HC and than cancelled without any reason. I also have 5 that are in different stages of review. I will be speaking to the head of the MMPR program next week to find out what is going on with the delays. My personal thought is that HC is waiting for an risk assessment on the impact of the Manson injunction on the MMPR before they start inspections again.
QA is becoming a black hole as HC learns from the submissions and see's some of the same names on applications. One of the big Exper QA companies has been told that they can't be everyone's QA and to stop it. They are just taking money and not doing a great job from what I have seen. My clients have been left in a jam by this company and that's why they came to me.
I just had another of my QA's associates approved by HC this week, the only issues we are dealing with is when they will be on site and for how long. YOU DO NOT NEED A QAP FULL TIME as of this writing.
People can reach me at pipedreemz at hushmail dot com, my team and I can help.
This is one of many HC letters I have addressed for my clients successfully and I have a pile of them, lol
Hello,
Thank you for your additional information regarding your quality assurance person, received April 2 2014 in regards to your application # 10-MM0003.
The quality assurance person that is designated under section 10 of the application can not delegate any responsibilities under Division 4 to another individual. This person is responsible to ensure quality at all steps and must ensure that dried marihuana is produced, packaged, labelled and stored in accordance with the SOPs developed, using the proper equipment and within the sanitation program established and all items under Division 4.
Currently the proposed schedule for QAP is unclear. Given that Mr. QAP is a Consultant, and that the production of marihuana usually extends over a long period of time from sowing of the seeds to drying the product and that production, packaging and labelling may be conducted on daily basis, your proposal still lacks in demonstrating how it will maintain the quality of all dried marihuana before it is made available for sale as per the requirements of Division 4 of the MMPR.
Please submit a more detailed description of the work schedule of your quality assurance person to ensure that all steps detailed above will be sufficiently overseen by this person.
As per section 58 of the MMPR, dried marihuana must be produced, packaged, labelled and stored
in accordance with standard operating procedures that are designed to ensure that those activities are conducted in accordance with the requirements of this Division. As per section 60, the quality of the product is the responsibility of the Quality Assurance person. Please confirm whether the quality assurance person is full-time or part-time and please provide additional information to demonstrate how they will be able to ensure the quality of the product at all steps.
The information requested must be submitted by
April 24 2014.
If you have any additional questions, please do not hesitate to send us your questions by email at
MMPR-RMFM@hc-sc.gc.ca.
Licences and Permits Division
Office of Controlled Substances
Health Canada