Good Manufacturing Practices Case Study Example | Topics and Well Written Essays - 750 words

Good Manufacturing Practices - character reference Study ExampleI am working in a Japanese pharmaceutical guild Takeda in Ireland. It is a research based largest pharmaceutical company in Japan and one of the international leaders of the industry. I consider it to be a privilage to be with such an esteemed organization. Basically, I am involved in dispensing raw materials and controlling coating process. The raw materials that ar the basic ingredients of any practice of medicine needs to be passed through GMP to be qualified, sourced properly, and tested before release into handling. Though these regulations vary in different part of the world, they are responsible to creating business and compliance challenges.Poor quality medicines or those medicines that are not manufactured using GMP can damage health. For instance, a poor quality medicine whitethorn contain toxic substances that commit been unintentionally added, causing damage to health or fifty-fifty death. The use of GMP is absolutely necessary in each and every step starting from selecting the raw materials till the death product is sealed and packed properly. If the coating of the drug is not good, it may loose most of its worthy ingredients by the time it reaches the consumer. It is a well known fact that a medicine that contains little or none of the claimed ingredient will not drop the planned therapeutic effect. I believe that ill luck to comply with GMP regulations can depart in very dear costs as well as product recall, seizure, termination of manufacture, fines, and even imprisonment. Every time we take a medicine we can have confidence that the medicine has been manufactured in accordance with GMP because it has today become a global standard. GMP on with expert assessment gives us a clear overview that every medicine is safe to use, will have the necessary efficiency and will be of the right quality (emeu.eu, N.D.). GMP or the recently updated cGMP, where the c corresponds to current, propel manufacturers that they must utilize technologies and systems which are modern and abide by with the regulation. Under current GMP rules and regulations which is the latest interpreting of GMP, it is the pharmaceutical manufacturer who is accountable for the entire operations (Saffron Media Pvt. Ltd., 2004). There are a variety of practices that mark quality some of them are as follows raw materials quality declaration maintaining correct substances all the dash through the manufacturing process standards for hygiene and safety in-house testing production and process controls and warehousing and distribution (Dietary auxiliary Quality Initiative, 1999). I am responsible for dispensing raw materials and controlling coating process. As a result of following GMP my working environment is much more safe and efficient. Additionally, these regulations require that manufacturers, processors, and packagers of drugs, to take positive steps to make sure that their product s are secure, unadulterated, and effective. GMP regulations necessitate an extremely good manufacturing process, allow companies to reduce or even eliminate probable chances of contamination, mixups, and errors. Failure of companies to meet the terms with GMP can result in very serious costs. Studies have shown that GMPs offer quality assurances that off-the-shelf testing cannot. In fact,