The main responsibility of the Food and Drug Administration is to inspect producers or processors that provide FDA regulated foodstuffs, and also to authenticate their act in accordance with the applicable set of laws. The core purpose of this organization is mainly related to medical products, food, global regulatory operations, and use of veterinary medicines and so on.
The CGMP is a kind of yardstick by the use of which the FDA decides whether the quality of a certain medicinal drug is safe for the consumers to use or not. FDA compliance leaders in the pharmaceutical industry for functioning of a drug are the ideal example of the how the work ethic of a particular medicinal drug manufacturing company should be.
Actions taken: The process to comply with cGMP requirements is a doubt that has to be dealt with really carefully by all the manufacturers of different medicinal drugs. The main body of FDA, for whom this CGMP serves as a yardstick for checking the quality of the products going to the consumers, especially medical drugs has the right to issue a written complaint against the accused company, if found guilty and send this company a warning letter.
The potential weak spots of the processes in the company must be identified immediately as it would attract the attention of the inspectors immediately. One or two individuals must be appointed who are able to administer every key development inside your competence and they should be qualified to escort an FDA delegate all through the assessment.
Processes involved here: The decisions which are taken in the CGMP regarding the manufacturing process of a certain product of a company is governed by different kinds of parameters. A very thorough and complete inspection of the facilities of the company, very careful examination and reexamination of the alleged product sample, under strict scrutiny is done. Also what is present in the back of the mind of the officer is the fact that how eventful is the history of the firm and careful examination, testing of the manufacturing processes and their subsequent evolution with the passage of time within the company itself. The reports which are put up in the CGMP should be made in accordance to the compliance policies created by the Federal regulations. All the different processes require careful inspection and even cross examinations later on.
The CGMP is a kind of yardstick by the use of which the FDA decides whether the quality of a certain medicinal drug is safe for the consumers to use or not. FDA compliance leaders in the pharmaceutical industry for functioning of a drug are the ideal example of the how the work ethic of a particular medicinal drug manufacturing company should be.
Actions taken: The process to comply with cGMP requirements is a doubt that has to be dealt with really carefully by all the manufacturers of different medicinal drugs. The main body of FDA, for whom this CGMP serves as a yardstick for checking the quality of the products going to the consumers, especially medical drugs has the right to issue a written complaint against the accused company, if found guilty and send this company a warning letter.
The potential weak spots of the processes in the company must be identified immediately as it would attract the attention of the inspectors immediately. One or two individuals must be appointed who are able to administer every key development inside your competence and they should be qualified to escort an FDA delegate all through the assessment.
Processes involved here: The decisions which are taken in the CGMP regarding the manufacturing process of a certain product of a company is governed by different kinds of parameters. A very thorough and complete inspection of the facilities of the company, very careful examination and reexamination of the alleged product sample, under strict scrutiny is done. Also what is present in the back of the mind of the officer is the fact that how eventful is the history of the firm and careful examination, testing of the manufacturing processes and their subsequent evolution with the passage of time within the company itself. The reports which are put up in the CGMP should be made in accordance to the compliance policies created by the Federal regulations. All the different processes require careful inspection and even cross examinations later on.
About the Author:
It was a pleasure working with PharmEng. They were very professional and able to grasp our Program and what we wanted to accomplish. They brought some great ideas and how to achieve it to meet the goals and complete the project effectively How to prepare for an FDA or Health Canada inspection.
