Good Manufacturing Practice GMP Guidelines Eudralex Volume 4
M. Dumpala. INTERNATIONAL JOURNAL OF TREND IN SCIENTIFIC RESEARCH AND DEVELOPMENT, 5 (6):
1461-1472(October 2021)
Abstract
The basic rules in any good manufacturing practice GMP regulations postulate that the pharmaceutical manufacturer must maintain appropriate documentation and records. Documentation helps to build up a detailed interpretation of what a manufacturing function has done in the past and what it is doing now and, thus, it provides a base for planning what it is going to do in the future. Regulatory evaluators, during their inspections of manufacturing sites, often devote much time on examining a company's documents and records. Effective documentation boosts the visibility of the quality assurance system. Mr. Rajesh. L. Dumpala | Mrs. Lakshmi Prasuna. R. Dumpala "Good Manufacturing Practice (GMP) Guidelines (Eudralex-Volume 4)" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-6 , October 2021, URL: https://www.ijtsrd.com/papers/ijtsrd47639.pdf Paper URL : https://www.ijtsrd.com/pharmacy/pharmaceutics/47639/good-manufacturing-practice-gmp-guidelines-eudralexvolume-4/mr-rajesh-l-dumpala
%0 Journal Article
%1 noauthororeditor
%A Dumpala, Mr. Rajesh. L. Dumpala | Mrs. Lakshmi Prasuna. R.
%D 2021
%J INTERNATIONAL JOURNAL OF TREND IN SCIENTIFIC RESEARCH AND DEVELOPMENT
%K 21 210 211 Agencies CFR Documentation GMP Part Regulations and
%N 6
%P 1461-1472
%T Good Manufacturing Practice GMP Guidelines Eudralex Volume 4
%U https://www.ijtsrd.com/pharmacy/pharmaceutics/47639/good-manufacturing-practice-gmp-guidelines-eudralexvolume-4/mr-rajesh-l-dumpala
%V 5
%X The basic rules in any good manufacturing practice GMP regulations postulate that the pharmaceutical manufacturer must maintain appropriate documentation and records. Documentation helps to build up a detailed interpretation of what a manufacturing function has done in the past and what it is doing now and, thus, it provides a base for planning what it is going to do in the future. Regulatory evaluators, during their inspections of manufacturing sites, often devote much time on examining a company's documents and records. Effective documentation boosts the visibility of the quality assurance system. Mr. Rajesh. L. Dumpala | Mrs. Lakshmi Prasuna. R. Dumpala "Good Manufacturing Practice (GMP) Guidelines (Eudralex-Volume 4)" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-6 , October 2021, URL: https://www.ijtsrd.com/papers/ijtsrd47639.pdf Paper URL : https://www.ijtsrd.com/pharmacy/pharmaceutics/47639/good-manufacturing-practice-gmp-guidelines-eudralexvolume-4/mr-rajesh-l-dumpala
@article{noauthororeditor,
abstract = {The basic rules in any good manufacturing practice GMP regulations postulate that the pharmaceutical manufacturer must maintain appropriate documentation and records. Documentation helps to build up a detailed interpretation of what a manufacturing function has done in the past and what it is doing now and, thus, it provides a base for planning what it is going to do in the future. Regulatory evaluators, during their inspections of manufacturing sites, often devote much time on examining a company's documents and records. Effective documentation boosts the visibility of the quality assurance system. Mr. Rajesh. L. Dumpala | Mrs. Lakshmi Prasuna. R. Dumpala "Good Manufacturing Practice (GMP) Guidelines (Eudralex-Volume 4)" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-6 , October 2021, URL: https://www.ijtsrd.com/papers/ijtsrd47639.pdf Paper URL : https://www.ijtsrd.com/pharmacy/pharmaceutics/47639/good-manufacturing-practice-gmp-guidelines-eudralexvolume-4/mr-rajesh-l-dumpala
},
added-at = {2022-03-05T13:31:25.000+0100},
author = {Dumpala, Mr. Rajesh. L. Dumpala | Mrs. Lakshmi Prasuna. R.},
biburl = {https://www.bibsonomy.org/bibtex/24a6b449b533a4aa73976668e7b02db92/ijtsrd},
interhash = {0b81695442011ebcdd22ceee73f9f2e1},
intrahash = {4a6b449b533a4aa73976668e7b02db92},
issn = {2456-6470},
journal = {INTERNATIONAL JOURNAL OF TREND IN SCIENTIFIC RESEARCH AND DEVELOPMENT},
keywords = {21 210 211 Agencies CFR Documentation GMP Part Regulations and},
language = {English},
month = oct,
number = 6,
pages = {1461-1472},
timestamp = {2022-03-05T13:31:25.000+0100},
title = {Good Manufacturing Practice GMP Guidelines Eudralex Volume 4
},
url = {https://www.ijtsrd.com/pharmacy/pharmaceutics/47639/good-manufacturing-practice-gmp-guidelines-eudralexvolume-4/mr-rajesh-l-dumpala},
volume = 5,
year = 2021
}