Welcome to LookChem.com Sign In | Join Free

Details

Home > Chemical Encyclopedia > Basic Chemical > Chemical Noun Definition >
 Good manufacturing practice(GMP)
  • Good manufacturing practice(GMP)
  • "Good manufacturing practice" or "GMP" is part of a quality system covering the manufacture and testing of pharmaceutical dosage forms or drugs and active pharmaceutical ingredients, diagnostics, foods, pharmaceutical products, and medical devices. GMPs are guidelines that outline the aspects of production and testing that can impact the quality of a 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 these guidelines remains more or less similar that is ultimate goal to produce a good quality medicine or medical devices or active pharmaceutical products.

    Although there are a number of them, all guidelines follow a few basic principles.

    ♦ Manufacturing processes are clearly defined and controlled. All critical processes are validated to ensure consistency and compliance with specifications.
    ♦ Manufacturing processes are controlled, and any changes to the process are evaluated. Changes that have an impact on the quality of the drug are validated as necessary. 
    ♦ Instructions and procedures are written in clear and unambiguous language. (Good Documentation Practices) 
    ♦ Operators are trained to carry out and document procedures. 
    ♦ Records are made, manually or by instruments, during manufacture that demonstrate that all the steps required by the defined procedures and instructions were in fact taken and that the quantity and quality of the drug was as expected. Deviations are investigated and documented. 
    ♦ Records of manufacture (including distribution) that enable the complete history of a batch to be traced are retained in a comprehensible and accessible form. 
    ♦ The distribution of the drugs minimizes any risk to their quality. 
    ♦ A system is available for recalling any batch of drug from sale or supply. 
    ♦ Complaints about marketed drugs are examined, the causes of quality defects are investigated, and appropriate measures are taken with respect to the defective drugs and to prevent recurrence. 
    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 company's responsibility to determine the most effective and efficient quality process.

    Other good practices

    Other good-practice systems, along the same lines as GMP, exist:

    ⇒ Good laboratory practice (GLP), for laboratories conducting non-clinical studies (toxicology and pharmacology studies in animals); 
    ⇒ Good clinical practice (GCP), for hospitals and clinicians conducting clinical studies on new drugs in humans; 
    ⇒ Good regulatory practice (GRP), for the management of regulatory commitments, procedures and documentation.
    Collectively, these and other good-practice requirements are referred to as "GxP" requirements, all of which follow similar philosophies. (Other examples include good agriculture practices, good guidance practices, and good tissue practices.) In the U.S., medical device manufacturers must follow what are called "quality system regulations" which are deliberately harmonized with ISO requirements, not cGMPs.


    Prev: Kashrut
    Next: International Organization for Standardization(ISO)
  • Back】【Close 】【Print】【Add to favorite
Periodic Table
    Hot Products