When I walk into a hydroponic retailer to introduce myself, and our fine line of automated trimming machines, I usually create a huddle of floor and over-the-counter sales reps, when I show them a video clip of our machines in action.

I love to see the reaction from the sales reps, when they group and gasp in awe of the precision trimming that our machines provide. However, when dialogue presents itself such as the security, time and the money saved that automated machines have vs. crews of hand bud trimmers, some reps begin to clam-up, or take a bit of a backward stance. Hmm.?

Well, not all have that bit of a hesitancy, so I may be over exaggerating a bit. But even though it’s a small morsel I started to begin to wonder why? Of course as a sales rep you want to dissect all objections and doubt, so I began to ask questions, but after checking into it, I than noticed that when bringing the subject up that it may sound a bit harsh, Why? Well I found out that most of these sales reps are hired hands of hand bud trimmers for some of their own customers. And that when you bring up the subject of why automated machines are in demand, well.

I began to take note when asking questions, and what I came up with, and of course with a bit of educating the masses and also intertwining their feedback, we were all in agreement that some hybrid Bud trimming has to still be involved in conjunction with automated trimming. Well, we all know for sure when you come across a nice dragon bud, that can probably win some award we definitely would think twice before throwing that in a machine.

They also acknowledged that their own customer base is looking for security, time and money saved and most of all piece of mind. As for the rest of all the hand bud trimmers that are still on the roster with their customers, well I’m sure they’ll be the ones to be counted on first to continue to hand trim the best of those golden dragons, those prized possessions from their customers crop.

Michael Garay ~

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.