Literature DB >> 18468382

Pharmaceutical GMP: past, present, and future--a review.

K T Patel1, N P Chotai.   

Abstract

Good Manufacturing Practice (GMP) is a set of regulations, codes, and guidelines for the manufacture of drug substances and drug products, medical devices, in vivo and in vitro diagnostic products, and foods. GMP term that is recognized worldwide for the control and management of manufacturing and quality control testing of pharmaceutical products. Everyone in the pharmaceutical industry should know the story of how the good manufacturing practices (GMPs) have come to be. Most requirements were put in place as responses to tragic circumstances and to prevent future tragedies. To obtain and maintain GMP compliance, one should know the precedent of the GMP. The present review highlights past, present and future of GMP.

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Year:  2008        PMID: 18468382

Source DB:  PubMed          Journal:  Pharmazie        ISSN: 0031-7144            Impact factor:   1.267


  3 in total

1.  Longitudinal study of the impact of three major regulations on the Korean pharmaceutical industry in the last 30 years.

Authors:  Seung In Um; Uy Dong Sohn; Sun-Young Jung; Seung-Hun You; Changone Kim; Sora Lee; Heesang Lee
Journal:  Health Res Policy Syst       Date:  2022-01-06

2.  An assessment of adherence to the WHO-delineated good manufacturing practice by the pharmaceutical companies in Kabul, Afghanistan.

Authors:  Rohullah Roien; Rajeev Shrestha; Kashikant Yadav; Akihiko Ozaki; M Bashir Ahmadi; Yudai Kaneda; Yasuhiro Kotera; Binaya Sapkota; Sunil Shrestha
Journal:  Cost Eff Resour Alloc       Date:  2022-04-02

3.  Clinical research regulation in India-history, development, initiatives, challenges and controversies: Still long way to go.

Authors:  Mohammed Imran; Abul K Najmi; Mohammad F Rashid; Shams Tabrez; Mushtaq A Shah
Journal:  J Pharm Bioallied Sci       Date:  2013-01
  3 in total

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