The Indo Expo is a premier cannabis trade show that takes place in Denver, Colorado. This is a full-spectrum B2B event that showcases a variety of products and tools from equipment and lighting to nutrition and more! This event features seminars, workshops, demonstrations, over 350 exhibitors and thousands of buyers, owners and master growers.

The event is split into two days: Saturday, January 26th is industry day for B2B relationships only and is followed by Sunday, January 27th which is open to the general public. This event is a great opportunity for individuals to learn more about cannabis and all the wonderful products available.

This year, CenturionPro Solutions is proud to be the Indo Expo 420 sponsor and we are excited to showcase our elite line of trimming machines yet again! Come by during the event to learn all about our elite bud trimming systems and even pick up some helpful tips and tricks. Make 2019 your year to be harvest ready with an elite CenturionPro trimmer at your side.

Visit us @ BOOTH 420!

The event is located at 451 East 58th Avenue, Denver (Expo Halls).

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.