Answer Posted / g. subrahmanyam
CFR is Code of Federal Regulations is the codification of
the general and permanent rules and regulations (sometimes
called administrative law) published in the Federal Register
by the executive departments and agencies of the federal
government of the United States. The CFR is published by
the Office of the Federal Register, an agency of the
National Archives and Records Administration (NARA). The
CFR is divided into 50 titles that represent broad areas
subject to Federal regulations. Out of 50 we will use
Title-21 which refers to Food & Drugs. Hence we call it as
21-CFR. This 21-CFR is further divided into 1500 parts.
Out of which we will be using frequently 11 (i.e. 21-CFR
Part-11) for Electronic records (i.e. 21-CFR Part-211) and
211 for Good manufacturing practices.
| Is This Answer Correct ? | 39 Yes | 0 No |
Post New Answer View All Answers
if you given one product then which tests you will perform?
How to determine water content of bis tetrazole amine mono ammonium salt
why we are using benzene, anyline in acetic anhdride assay titration method?
Why Ethanol is Used for Standardization of GC Head space?
in hplc chromatogram started from left to right and in uv spectrum started from left to right
What is the purpose of octyl silane columns?
How we choose the mobile phase for method development.?
why lactose has less charges when packed in steel containers when compared with packing of lactose in polyamide material?
[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
how you confirm the assay method?
Related substance method equivalency on control sample or spiked sample?
We use Potassium Dichromate solution for the calibration of UV-Visible Spectrophotometer in UV region. My question is to calibrate visible region which solution could be used in photometric accuracy
Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
How do we quantify crystaline and amarpous forms by using (NMR, XRD)spectroscopic techniques? Which any others instruments are useful for this quantification? explain
in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?