Marijuana Quality Control Plan / Cannabis Quality Control Procedures
Sample Quality Control Procedure pages:
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Plans are non-refundable, but you can see the WHOLE THING before you buy! Contact Jennifer now to schedule a screen share preview. Quality Assurance is the process and set of protocols that a cannabis production company follows to ensure that flower material and derivative products are consistent and safe to consume. In a highly regulated setting, the protocols can be intensive. Most license applications require submission of a Quality Control Procedure or Quality Assurance Plan so the applicant can prove to government regulators that appropriate measures have been considered and implemented. This includes proper measuring of substances, cross-checking of all documentation, packaging and labeling standards, and many other components. Disclaimer: This is a template that will be delivered to you as an editable MS Word doc. It's filled in with great information, but is NOT location specific. We've done 90% of the heavy lifting, and the last 10% is up to you and your compliance expert. |
Hi, I'm Jennifer Martin, the creator of this website and a veteran commercial grower and cultivation consultant. My colleague and I created these operating plan documents to help cannabis business operators legitimize and streamline their operations. With hundreds of satisfied customers under our belts, we are certain that we've got the best starter templates for cannabis operators available online.
Unlike other cannabis websites, this business is owner operated and I personally stand behind the quality of the available products and services.
This 19-page Quality Assurance template is suited for projects in the pre-license phase of a cannabis production project. It is meant to get your started in meeting the QA/QC regulatory requirements of your local jurisdiction.
Table of Contents
Introduction 3
Roles and Responsibilities 5
Quality Assurance Officer 5
Quality Control 6
Plant Inspection 7
Equipment 7
Internal Sampling and Testing 9
Packaging and Labeling 10
Audits 11
Adverse Event and Recall Plan 12
Adverse Event Planning 12
Adverse Event Recording & Investigation 13
Information gathering: 13
Distribute gathered information 14
Notify others as soon as possible 14
Secure unsold items from the specified batch(es) 14
Investigate 14
Develop a response and notify others 15
Recall Plan 16
Adverse Event Documentation 17
Reporting Requirements 17
Quality Assurance/Quality Control Training 18
General Training 18
Adverse Event Team 19
Training Support 19
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