enow.com Web Search

Search results

1. Results from the WOW.Com Content Network

2. Dissolution testing - Wikipedia

   en.wikipedia.org/wiki/Dissolution_testing

   In United States Pharmacopeia (USP) General Chapter <711> Dissolution, there are four dissolution apparatuses standardized and specified. [6] They are: USP Dissolution Apparatus 1 – Basket (37 °C ± 0.5 °C ) USP Dissolution Apparatus 2 – Paddle (37 °C ± 0.5 °C) USP Dissolution Apparatus 3 – Reciprocating Cylinder (37 °C ± 0.5 °C)

3. Talk:Dissolution testing - Wikipedia

   en.wikipedia.org/wiki/Talk:Dissolution_testing

   I think it would make the article clearer if "dissolution" was explained. CBHA 03:22, 10 May 2013 (UTC) [] @CBHA: A good suggestion but I disagree. Dissolution testing is a common name used in the Pharma industry, it should be pretty self-evident to most readers what dissolution means even if your not sure or don't work in that field ( a simple Google search can rectify any doubts).

4. Biopharmaceutics Classification System - Wikipedia

   en.wikipedia.org/wiki/Biopharmaceutics...

   The solubility classification is based on a United States Pharmacopoeia (USP) aperture. The intestinal permeability classification is based on a comparison to the intravenous injection. All those factors are highly important because 85% of the most sold drugs in the United States and Europe are orally administered. [citation needed]

5. United States Pharmacopeia - Wikipedia

   en.wikipedia.org/wiki/United_States_Pharmacopeia

   The USP is published in a combined volume with the National Formulary (a formulary) as the USP-NF. [2] If a drug ingredient or drug product has an applicable USP quality standard (in the form of a USP-NF monograph), it must conform in order to use the designation "USP" or "NF".

6. Sink condition - Wikipedia

   en.wikipedia.org/wiki/Sink_condition

   In pharmaceutics, sink condition is a term mostly related to the dissolution testing procedure.. It means using a sheer volume of solvent, usually about 5 to 10 times greater than the volume present in the saturated solution of the targeted chemical (often the API, and sometimes the excipients) contained in the dosage form being tested.

7. USP 800 - Wikipedia

   en.wikipedia.org/wiki/USP_800

   USP 800 (Hazardous Drugs—Handling in Healthcare Settings) is a guideline created by the United States Pharmacopeia Convention (USP), as one of their General Chapters through which the USP "sets quality standards for medicines, dietary supplements and food ingredients".

8. Template:NFPA 704 diamond - Wikipedia

   en.wikipedia.org/wiki/Template:NFPA_704_diamond

   This template produces a NFPA 704 safety square with optionally four hazard codes. It is designed to be used in a table. It is designed to be used in a table. Primary use is through {{ Chembox }} , the {{ NFPA 704 }} box and {{ OrganicBox complete }} (chemical data pages).

9. Orsat gas analyser - Wikipedia

   en.wikipedia.org/wiki/Orsat_gas_analyser

   An Orsat gas analyser or Orsat apparatus is a piece of laboratory equipment used to analyse a gas sample (typically fossil fuel flue gas) for its oxygen, carbon monoxide and carbon dioxide content. Although largely replaced by instrumental techniques, the Orsat remains a reliable method of measurement and is relatively simple to use.