GMP


Topic Replies Activity
Weight variation of tablet & capsule 1 November 5, 2019
How many HEPA filters will be placed in a clean room? and where it should be placed? 4 June 13, 2019
Expiry date for the raw materials 3 June 13, 2019
Process Analytical Technology (PAT) 2 May 6, 2019
Heating , ventilation and Air conditiong system 4 March 22, 2019
What is the responsibility of technical supervisor in production unit 4 March 21, 2019
ASQ CertifiedcGMP Professional 1 January 7, 2019
Equipment change in facility 3 November 22, 2018
What action to be taken if an OOT result is confirmed 8 September 10, 2018
Garment according to the clean room 3 September 6, 2018
What is purpose of cross over bench in change room? 3 August 1, 2018
What is glass policy please understand in briefly 6 July 11, 2018
Equipment Gap Analysis and remediation plan 3 June 30, 2018
Production environment in GMP WHO 1 June 5, 2018
How to conduct audit in HEPA filter 3 April 20, 2018
GMP guidelines for Active Pharmaceutical Ingredients (APIs) 2 February 6, 2018
Mfg plant construction 1 December 30, 2017
Production reworking 1 December 15, 2017
GMP principals for hazardous drug manufacturing 1 November 4, 2017
GMP correction in executed documents 5 June 24, 2017
Good documentation practices 1 April 28, 2017
Paper shredder SOP 1 April 4, 2017
Need to know data integrity part of SOP 1 February 13, 2017
ICH Q7 Good Mfg practice API 2 October 13, 2016
GMP certification 1 June 4, 2016
Distance between Cephalosporin & general product plant 1 June 2, 2016

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