I like hand trimmed buds as much as the next person, however I honestly believe that hand trimmed buds will become a rarity in the near future. Unless hand trim is something you specialize in, from just about any standpoint, machine trimming is the only future the harvest world can expect. It is more cost effective and would allow dispensaries to hire their own tight harvest teams. Machine operators on average make more than a base level trimmer, and allows for the entire batch of each strain to have the same level of quality. Larger dispensaries in the state hire out to harvest specialists that use trimming machines such as Hemp Temps and Colorado Trim. These companies maximize their profits by having these tighter crews of more experienced workers. Hand trimming while utilizing machines would be the best hybrid, with the larger buds on the stem being hand trimmed for bag appeal. While there are many machines on the open market, after extensive research and trial and error, the superior machine on the market seems to come from Centurion Pro Solutions. With Centurion trimmers concentrates and trim weight retention have never been higher. With the dual catch bag, two new products are created for use in concentrates and edibles. The inner 200 micron bag collects any heavier materials, perfect for edibles or bag washes for bubble hash. The outer bag catches all fine material like trich matter and what some people lovingly refer to as kief. This kief can be easily ran through any number of concentrate processes either pressing for Rosin or blasting for Oil. Either can be accomplished with great efficiency and no risk to the outcome of the final product, due to the Centurions revolutionary Quantanium tumbler which requires no Clear Cut or hemp oil of any kind. All together the machine is a huge time and money saver. Especially compared to other high volume bud trimmers in this similar horizontal style trimming.

~Connor

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.