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Good documentation practice (recommended to abbreviate as GDocP to distinguish from "good distribution practice" also abbreviated GDP) is a term in the pharmaceutical and medical device industries to describe standards by which documents are created and maintained.
In Europe GDP is based on the Commission Directive (EU) 2017/1572 of 15 September 2017 supplementing Directive 2001/83/EC of the European Parliament and of the Council as regards the principles and guidelines of good manufacturing practice for medicinal products for human use.
GxP is a general abbreviation for the "good practice" quality guidelines and regulations. ... Good distribution practice, or GDP; Good engineering practice, ...
Volume 7 - Guidelines. Volume 8 - Maximum residue limits. Concerning Medicinal Products for Human and Veterinary use: Volume 4 - Good Manufacturing Practices. Volume 9 - Pharmacovigilance. Miscellaneous: Guidelines on Good Distribution Practice of Medicinal Products for Human Use (94/C 63/03)
Good distribution practice (GDP) deals with the guidelines for the proper distribution of medicinal products for human use. Good laboratory practice (GLP), for laboratories conducting non-clinical studies (toxicology and pharmacology studies in animals) Good pharmacovigilance practice (GVP), for the safety of produced drugs
Drugs are classified under five headings. Under retail and distribution: [citation needed] Schedule X drugs - narcotics; Schedule H and L - injectables, antibiotics, antibacterials; Schedule C and C1 - biological products, for example serums and vaccines; Under manufacturing practice:
Gidea Park railway station, National Rail station code GDP; Good distribution practice, the guidelines for the proper distribution of medicinal products for human use; Global Drifter Program, a program that was aiming to collect measurements of surface ocean currents, sea surface temperature and sea-level atmospheric pressure using drifters.
The Principles of Good Laboratory Practice (GLP) establish rules and criteria for a quality system that oversees the organizational processes and conditions in which non-clinical health and environmental safety studies are planned, conducted, monitored, recorded, reported, and archived.