Customer complaints against a cannabis pharmaceutical company must be taken seriously. Not only is it part of GMP — Good Manufacturing Practices — but the potential for lawsuits can be heavy in this new industry that is still largely unregulated.
Let’s face it. Accidents happen and people make mistakes. That being said, a good Quality System and Safety Program will continuously seek out potential areas of risk and patch the areas by implementing change control and process improvement. These practices are widely known throughout the compliance-world as HACCP – Hazards and Critical Control Points. While there are external factors that you may have little control over, the more you consider risk ahead of time and what procedures to put in place to prevent them from happening in the future, the less likely there will be large financial losses for your company.
People who are consuming cannabis products for any reason must be careful when searching for a quality pharmacy that provides safe and legal sources of cannabis products. No matter what types of products they’re seeking—dried, oil, extract, butter, etc.—these products should have been produced through GMP—Good Manufacturing Practices. One of the best ways to determine if a cannabis product follows safety compliance for consumption is through a CoA, or Certificate of Analysis.
When you’re setting up your manufacturing facility you want to know that it will conform to all regulations and certifications to ensure that you only sell the most effective and safe products to dispensaries. There are many different terms you may hear when doing your research. You may have heard how you need a quality assurance department and a quality control department. They sound similar, but both play much different roles in a facility. If you want to run a successful operation than both are also necessary.
Well folks, it finally happened. The FDA raided a CBD Manufacturing Site.
This wasn't the first presence that the FDA had in the CBD world. Several warning letters have been distributed over a course of the past few years - all of them focused on improper marketing by the CBD companies in which claims were made that the products could cure, mitigate, or treat diseases.
If you’re in the process of setting up a small cannabis-related company, now is the best time to start GMP, or Good Manufacturing Practices. Not only do these help with the efficient operation of your manufacturing facility, they can help with every aspect of your operation, including helping to license and regulate your operation.
It’s important to stay on top of GDP–Good Documentation Practices–so that your cannabis business can comply to FDA and other government regulations. Good documentation practices are an important tool that can be used in your company’s compliance with the FDA and other government agencies responsible for the current or future licensing of cannabis products, state-wide or federally.
If you’re running a cannabis or dietary supplement type of GMP production facility, then your products are reliant on being sold well before expiry dates. Failure to manage this means that you’d have expired stock on shelves that can cost you losses and can also compromise the safety of the products you’re providing to the consumer market. FIFO is the industry standard in food production safety.
A lab coat worn by workers in a cannabis product or dietary supplement manufacturing facility needs to follow specific requirements. These are very similar to food manufacturing facilities too. Instead of requiring your personnel to buy their own lab coats, the GMP production facility should be providing ones for their lab workers and production line workers to prevent any issues.
Having your cannabis manufacturing facility follow GMP–Good Manufacturing Practices–can save you money in the long run. It’s tempting to try and cut corners by operating without a QA department, but you should be aware that there are many concerns that can cost you money and consumer trust in the longterm.
Wherever there are humans there will be pests. Pests love to follow humans, as we provide them with a ready source of food. Often pests are attracted to outdoor disposal bins, before heading indoors to warmth and a ready access of food. If you’re running a GMP production facility then you’ll need to take pest control seriously.
When you run a GMP production facility that includes cannabis and dietary supplement products, there are certain processes that you must follow in order to achieve government compliance. Cannabis products should follow similar guidelines in food processing and the pharmaceutical industry. This includes qualifying equipment before using it to produce food or medicine.
If you’re running a cannabis manufacturing facility there will be new government regulations ahead. It’s important to stay in compliance and obtain the expertise of GMP advisors who can guide you through setting up a sanitary and productive facility. If your facility has received a customer complaint it’s important to take it seriously.
A quality assurance system is a huge undertaking, but many of the components are actually common sense. Sometimes, just interpreting these requirements and breaking them down into systematic steps is all you need to get started. Becoming a GMP facility can take a year, or even more. So it’s important to know where to start. Here are a few tips to help you achieve an effective quality assurance system from the ground up.
In order to obtain GMP certification you’ll need to learn how to communicate effectively with your GMP auditor. This is an important national certification that provides a standard of quality insurance to show other companies that your cannabis products are safe and pure. However, undergoing an audit can be a stringent and rigorous process. Perhaps the audit will be the toughest part of setting up a new cannabis manufacturing business.
One of the steps toward achieving cannabis compliance for is by assessing shelf life. Stability studies are required in GMP and are vital to any quality assurance system. Expiration dates will need to be printed onto product packaging in order to protect consumers and your company by ensuring the quality of a product through a specific time.
If your cannabis or dietary supplement business is in production, you’ll need to ensure that you keep excellent records to document and guide each step of manufacturing. The batch production record, or BPR, is one of the most important forms that your facility workers will need to fill out. Batch production records are a crux of any quality assurance system and are necessary to abide by Good Manufacturing Practices, or GMP.
Buying on the black market has never been safe for consumers, regardless of whether the purpose is recreational or pharmaceutical. Most people who use cannabis medically or recreationally are not able to trace where their product came from, if it was grown without harsh chemicals, or if it is pure and does not contain “laced” or added ingredients to enhance psychoactive effects.