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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 the US, Good Manufacturing Practice (GMP) Regulations are based on the Code of Federal Regulations 21 CFR 210/211, and USP 1079. The US Drug Supply and Chain Security Act (DSCSA), was enacted by Congress on November 26, 2013 and outlines requirements to build electronic systems that identify and trace prescription drugs distributed in the US ...
Deutsch; Ελληνικά ... Volume 4 - Good Manufacturing Practices. ... Guidelines on Good Distribution Practice of Medicinal Products for Human Use (94/C 63/03 ...
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.
Good clinical practice, or GCP; Good documentation practice, or GDP, or GDocP (to distinguish from "good distribution practice") Good distribution practice, or GDP; Good engineering practice, or GEP; Good financial practice, or GFP; Good guidance practice, or GGP [5] [6] Good hygiene practice, or GHP; Good hygiene practice, or GHP; Good ...
Gross domestic product (GDP) is the market value of all final goods and services from a nation in a given year. [2] Countries are sorted by nominal GDP estimates from financial and statistical institutions, which are calculated at market or government official exchange rates.
In the United States, regulation of drugs was originally a state right, as opposed to federal right. But with the increase in fraudulent practices due to private incentives to maximize profits and poor enforcement of state laws, the need for stronger federal regulation increased. [7]
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.