Topic Replies Activity
Instructions Before You Start - Must Read 1 March 4, 2016
Microbial cleaning valdiation - non sterile production and packaging 2 November 12, 2019
LOQ determination through signal to noise ratio 3 November 12, 2019
End point of RMG & FBD 9 November 12, 2019
Water for injection 1 November 12, 2019
Tinidazole Tablet friability problem 2 November 11, 2019
Preparation of BMR 3 November 11, 2019
Temperature excursion of incubator under incubation plates 5 November 11, 2019
Compressed air validation 1 November 11, 2019
Export of pharmaceutical FDF from India 1 November 11, 2019
Microbilogical Purified water analysis as per usp and Bp 1 November 11, 2019
About before change control close can used equipment 2 November 10, 2019
Formulation of Clomiphene citrate 4 November 10, 2019
Dissolution of clomiphene citrate Tablet 9 November 10, 2019
Tablet Granulation 4 November 9, 2019
Water for injection temperature 80c 1 November 9, 2019
Type of Analysis in quality control 4 November 8, 2019
Viable and non viable count observation during batch filling.batch 3 November 8, 2019
Maximum Batch size for Terminal Sterilized Vial fill Injectable product 1 November 8, 2019
Required herbal product registration guideline for Burkina,Cameroon and IVC 1 November 7, 2019
Audit trail & instrument logbook 2 November 7, 2019
Pass box dynamic and static 1 November 6, 2019
Compressed air and Nitrogen Quality Parameter 3 November 6, 2019
Microbiology role in pharmaceutical industry 2 November 5, 2019
Change over room for QC 5 November 5, 2019
Qualification of a new laboratory 4 November 5, 2019
Cleaning validation 2 November 5, 2019
Weight variation of tablet & capsule
GMP
1 November 5, 2019
Utility Pipe Lines 3 November 5, 2019
Dispensing order 3 November 5, 2019

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