Sertifikasi GMP (Good Manufacturing Practice) – A good manufacturing practice (GMP) is a production and testing practice that helps to ensure a quality product. Many countries have legislated that pharmaceutical and medical device companies must follow GMP procedures, and have created their own GMP guidelines that correspond with their legislation. Basic concepts of all of these guidelines remain more or less similar to the ultimate goals of safeguarding the health of the patient as well as producing good quality medicine, medical devices or active pharmaceutical products. In the U.S. a drug may be deemed adulterated if it has passed all of the specifications tests but is found to be manufactured in a condition which violates current goo manufacturing guideline. Therefore, complying with GMP is a mandatory aspect in pharmaceutical manufacturing.
Although there are a number of them, all guidelines follow a few basic principles:
GMP guidelines are not prescriptive instructions on how to manufacture products. They are a series of general principles that must be observed during manufacturing. When a company is setting up its quality program and manufacturing process, there may be many ways it can fulfill GMP requirements. It is the companys responsibility to determine the most effective and efficient quality process.
INFORMASI & REGISTRASI
The Royal Palace Block A20
Jln. Prof.Dr. Soepomo, SH. Kav 178A, Jakarta 12870
Phone: (021) 8379 2006, (021) 8378 9513
Fax: (021) 8378 9538