The MJBiz Conference began in 2012 and is a cannabis business expo and conference featuring the world’s largest gathering of industry executives and experts. By 2016, this expo was recognized as being the fastest-growing trade show in the country!

With over 1,000 different exhibitors and 20,000 cannabis professionals in attendance, MJ Biz offers one of the greatest opportunities in the cannabis industry. This conference features growers of all sizes, as well as cannabis dispensaries and retailers, hydroponic stores, new technology in the growth and extraction sectors as well as infused cannabis products and legal services.

The Fall event is back in Las Vegas this November!

Las Vegas Convention Center

November 14 to November 16th

Visit Us @ Booth 2859

CenturionPro Solutions is †excited to be back this year to showcase our elite trimming machine lineup – including our brand new CenturionPro 3.0 triple barrel medical grade trimmer!

We will be available all weekend to answer questions and educate the industry on the CenturionPro Trimming Advantage. We hope to see you there!”

GMP refers to the Good Manufacturing Practice Regulations promulgated by the US Food and Drug Administration under the authority of the Federal Food, Drug, and Cosmetic Act (See Chapter IV for food, and Chapter V, Subchapters A, B, C, D, and E for drugs and devices.) These regulations, which have the force of law, require that manufacturers, processors, and packagers of drugs, medical devices, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective. GMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, mixups, and errors. This in turn, protects the consumer from purchasing a product which is not effective or even dangerous. Failure of firms to comply with GMP regulations can result in very serious consequences including recall, seizure, fines, and jail time.

GMP regulations address issues including record keeping, personnel qualifications, sanitation, cleanliness, equipment verification, process validation, and complaint handling. Most GMP requirements are very general and open-ended, allowing each manufacturer to decide individually how to best implement the necessary controls. This provides much flexibility, but also requires that the manufacturer interpret the requirements in a manner which makes sense for each individual business.

GMP is also sometimes referred to as “cGMP”. The “c” stands for “current,” reminding manufacturers that they must employ technologies and systems which are up-to-date in order to comply with the regulation.