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.
Recently, I took a trip to DC for the Vape Technology Association’S (VTA) FDA conference. I was invited to attend on the suggestion of a very political friend of mine that is in the industry. Being a non-political part of this industry,
Last weekend in Pasco, Washington, West Coast Vape Expo hosted a convention to help bring awareness and help raise money for the advocacy of vaping.
Here is a listing of common documentation that will be needed to prove your products timeline for PMTA. Remember this is not a “one size fits all” approach.
