The MJBiz Conference is a cannabis business expo and conference featuring the world’s largest gathering of industry executives and experts. MJBiz Con began in 2012 and, by 2016, was recognized as the fastest-growing trade show (out of all industries) in the country!

The MJBiz Conference offers the cannabis industry individuals and businesses the ability to network with thousands of industry leaders. With over 110 speakers, a minimum of 650 different exhibitors and 14,000 cannabis businesses in attendance, it is a testament to the industry itself. With everyone from medium to large wholesale growers, dispensaries, retailers, grow technology, extraction technology, infused cannabis products and even legal services, this event is ideal for building connections.

Visit Us @ Booth 233

The Spring event is in New Orleans and takes place from May 9 through to May 11. CenturionPro is proud to be exhibiting once again this year and showcasing our elite trimmer lineup! Come and visit us at Booth #233 to learn more about our automated machines – and meet our brand new CenturionPro 3.0 triple barrel trimmer!

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.