It won't be that much cuz it's 30 times the daily script or 150 g's a month whichever is less or the licence get's yanked. But the gray market will definitely be there.
That sort of central registry system would be the way to go, it would make picking an LP so much easier for people, doctors would not be pissed, and other doctors would not gauge people for scripts. Now, mind you that we'll have folks complaining that their data is in a "mainframe" somewhere and...
Correct me if I'm wrong but where in the regulations does it state that you have to be locked in for 1 year with a producer? All I see is that the registration of a client is valid for a year and needs to be renewed annually etc.
I think they will go up. You have to also factor in the possibility of the government slapping some sort of excise tax. Perhaps we'll go into something like the wine business, where you can make your own at home, grow your own at a facility, or purchase from a producer. Each has it's merits and...
I would tend to agree...I think we'll get closer to the U.S. standard, once marketing restrictions are relaxed, operations grow, competition gets more fierce, there will pressure to have bigger budgets to cover all of that and the money has to come from somewhere.
I'll try to call my contact at GLM tomorrow to see what's up, or to see if they are at liberty to discuss at least.
Again I have to agree that they are going to be back and fairly soon , the amounts of investment and time put into the operation is not something you do to make a quick buck and...
Yes I would definitely ask this contact of yours. She sounds like she has the hands on experience with QC, this is what HC wants.
We also knew our QC on a personal level.
Stigma: perhaps but we now have the former Ontario minister of health getting into the business, that should change...
Konrad,
We're in Ontario. You basically do not need to give them the everyday lifecycle of the plant. What they want to see rather is that you know what you are doing, and that you will follow the provisions of the MMPR and your procedures prevent the endangerment of health of your employees and...
Glad you are taking the plunge. I can tell you about what we have in house so you have some idea of how others are going about it. (Perhaps someone else can chime in about their stuff).
Our QAP is an in house staff member with a masters in microbiology. With years upon years of laboratory qap...
AA: Proving Grounds is only a few months old. AA3, 2.8 etc. are old as heck but the latest verison AA: PG is actually pretty good. The new devs are listening to the community. Give it another shot you might like it.
No we have not received what you refer to as a the phase 3 directive. But as I mentioned our premises are ready to go. The only thing holding us up was a regulatory technicality, which we've now met. So a build directive in our case is a 2 week project
You can build without their explicit ok...
From the conversations I've had with LP's and from the landscape I'm seeing there is room for Tweed type operations who will cater to a certain market, guys in between like PNP (although they are closer to Tweed then the other way) and smaller niche market players like some guys from the west...
We had our file pulled from RCMP and it was processed within 3 days in August. We received a note about clearance being done about a month and a half ago. So from the time RCMP sends their report to HC and the time it's processed can be months and months (in the mean time we had some adjustments...