Quality Assurance


Topic Replies Activity
Document Retention period 5 March 31, 2020
Multiple Batches 1 March 31, 2020
Qualification of Cold Storage facility 1 March 30, 2020
Primary packing supplier change and Stability study requirement 2 March 30, 2020
Calculation on anhydrous basis 6 March 24, 2020
Process validation 4 March 24, 2020
When i have to distribute the new sop to concerned department 3 March 21, 2020
Actual weight and conventional mass 4 March 20, 2020
Stability calculation 3 March 20, 2020
How to store narcotic substances 2 March 17, 2020
Stand alone CAPA 4 March 13, 2020
Incidents & Deviations 2 March 4, 2020
How can prepare the EQ OQ PQ Protocols for pulverizer equipment 2 February 29, 2020
How to convert obsolete version BPR to live 1 February 27, 2020
Qus. For future 1 February 26, 2020
Line clearance perameter 4 February 24, 2020
Procedure for destroying expired products 3 February 24, 2020
Validation of compressed air 2 February 24, 2020
Qulity warning letter for operators 3 February 15, 2020
Change control in pharma 2 February 13, 2020
Hold time study for inprocess and bulk products 1 February 13, 2020
Case label procedure SOP 1 February 12, 2020
Preparation of BMR 9 February 11, 2020
SOP categories in pharma 5 February 11, 2020
Quality by design 1 February 11, 2020
Visual Inspection Limits of ampules & vials 3 February 6, 2020
SOP Effective with open change control 3 January 29, 2020
GSM of PVDC foil 1 January 29, 2020
Leak test related questions 8 January 26, 2020
Disinfectant used 3 January 26, 2020

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