FDA (Food and Drug Administration) is the Government authority in USA that governs almost every manufacturing unit in terms of guidelines and compliance with proper manufacturing standards for any medical or any other manufacturing agency. Once the manufacturing unit is manufacturing within the standards set by the FDA regulations, you can expect a visit from a representative from FDA. This representative will make sure that proper standards and measures are followed in the manufacturing unit. They will, inspect your manufacturing unit and then they will submit an audit report to higher authorities.
Whenever an FDA authorized personal inspects any manufacturing unit, they take into account all their standards and compare if each and everything in the manufacturing unit is being properly followed or not and if all the guidelines are implemented. If you are into GMP (Good Manufacturing Practice) you have to be very well aware of all the guidelines of GMP.
GMP Trends® newsletter provided by us is one of the sources and real help in understanding any and all guidelines a manufacturer has to follow, that falls under FDA. The authorized personal will survey your plant or manufacturing unit and then submit the report to FDA.
GMP Trends® news letter covers everything related to this complex and very important issues of guideline and complaints for every FDA certification. If you are into manufacturing of various medicines and other medical equipments then, you also have to maintain the necessary compliance and guidelines as per the FDA. Now the question arises that how to do you know all these guidelines and compliance of FDA? We at GMP Trends® have a solution for it; we publish this GMP Trends® newsletter every month which have all the answers you would be looking for regarding the compliances and guidelines of FDA. Go out there and book your copy of GMP Trends® news letter for every month and you can also be updated over all the recent changes and new guidelines of FDA.