GMP pertains to the Good Manufacturing Practice Regulations which is being promulgated by the US FDA under the authority of Federal Food, Drug and Cosmetic. Such regulations that are under the force of law necessitate processors, manufacturers, and packagers of medical devices, drugs, blood and some food take the proactive steps to make sure that every product they make is pure, effective and safe.
The Gmp Regulations call for a quality approach to the process of manufacturing, allowing companies to eliminate or minimize cases of errors, contamination and mix ups. In turn, this will protect the consumers from buying a product which is ineffective or even dangerous. Firms who fail to comply with the GMP regulations may lead to extremely serious consequences such as fines, jail time, seizure and recall.
GMP regulations also address problems such as personnel qualifications, record-keeping, cleanliness, sanitation, process validation, equipment verification and complaint handling. Majority of the GMP requirements are very open-ended and general, letting every manufacturer to decide individually how to rightfully implement the required controls. It offers better flexibility but also requires manufacturers to interpret all requirements in such a way that will make sense for every individual business.
At times, GMP is also being called as cGMP wherein in c means current, which reminds manufacturers that they need to employ systems and technologies that are updated in order to adhere to the regulation. Equipment and systems used for preventing contamination, errors and mix ups, which could have been top of the line two decades ago, may already be less than sufficient by the present standards of today.
GMP covers every aspect of production, right from the starting materials, equipment and premises to the personal hygiene and training of staff. Written and detailed procedures are important or every process which could have an impact on the quality of the final product. There should be systems to ensure that there is documented proof which can show that correct procedures are being followed consistently at every step in the process of manufacturing each time a product is being made.
Needless to say, GMP is important no matter what the product in question might be and cetrimides are definitely not an exception. As far as the world of chemicals is concerned, cetrimides can disrupt the growth of any harmful fungi and bacteria through interrupting their normal functions. The processed food products, like meat and bread, contain the quaternary ammonium compounds of Cetrimide that act as a preservative.
With the right phase transfer catalysts, the cetrimide helps in keeping foods fresh much longer through the regulation of pH balance or acidity. Ammonium preservations are great antiseptic agents. The cetrimide is a very active ingredient in the specialty shampoos for treating dandruff, psoriasis and eczema. This is also being used in the industry of pharmaceutics to fight the soften and state paper products as well as bind detergents. The cetrimide is also an active ingredient found in the topical first aid creams. The antiseptic properties that cetrimide has helps in the prevention of infection in the open wounds like scrapes and cuts and this is soothing for chapped hands and diaper rash as well. Through GMP, there is a guarantee that cetrimide is produced and manufactured in the safest and most hygienic way possible to keep up with the industry standards.
Tatva Chintan Pharma Chem Pvt. Ltd, a leading raw material supplier for various pharmaceuticals companies in India and abroad has a wide variety of various chemical products like specialty chemicals, quaternary phosphonium salts, methylating agents, electrolyte chemicals, etc. It has made a name for itself with the kind of quality it provides at such a competitive price. The quality product supplied by them at such an affordable price has made them a big hit in the industry.
This post first appeared on Cetrimide | Phase Transfer Catalyst | Tetraethylammonium Tetrafluoroborate, please read the originial post: here
