Hey guys, a lot of my clients are ramping up for PMTA. In this vector it really does take a village, and it is important that we know who is on our side.
With so much talk about the FDA today, I see people forgetting about another crucial regulatory body that may be more likely to visit your facility (and report a problem).
One thing I have noticed going over registration and product listing files is the large amount of misleading information.
Whether you run an e-liquid vaping facility or you enjoy vaping, many people don’t understand the hazards of tossing vaping products into the garbage. E-liquids is the main concern.
Even if you’ve made a major investment in your vaping business and your premises, it’s important to focus on your next most valuable investment—your employees.
A batch record or batch production record can be one of the most important forms that your employees should be filling out.
Hello Vape Community,
While speaking with some industry leaders today, I noticed a deafening need for contract review. Contracts are the backbone of all manufacturing, whether food, cosmetic, or pharmaceutical.
Everyone can agree that July 28th was a big day for the vape industry. After one week of talking in DC with capitol hill about solidifying vape policy, FDA held a press conference.
These changes are positive and necessary but we as an industry might not be ready to move forward. Vape Manufacturers may not be as close to GMP as they once thought, others have mistook ISO as a GMP compliant process, but they couldn’t be more wrong.
If you’ve decided to open your own vaping products laboratory or plant, it can involve a complex system of practices. Laboratory procedurals will need to be set into place.