|
Process vlidation
|
|
7
|
1046
|
May 5, 2020
|
|
Drug and cosmotic rule
|
|
0
|
543
|
May 5, 2020
|
|
Recommissioning of equipment
|
|
3
|
776
|
May 3, 2020
|
|
Balance qualification
|
|
2
|
1765
|
May 2, 2020
|
|
Bioburden analysis
|
|
1
|
668
|
May 1, 2020
|
|
IPQA During Production
|
|
1
|
637
|
May 1, 2020
|
|
PH of the resulting solutions
|
|
1
|
598
|
May 1, 2020
|
|
Drug substance storage condition
|
|
1
|
694
|
May 1, 2020
|
|
cGMP Related doubts
|
|
1
|
673
|
May 1, 2020
|
|
Continual process verification
|
|
1
|
632
|
May 1, 2020
|
|
SOP FOR GOOD DISTRIBUTION PRACTICES
|
|
1
|
2177
|
May 1, 2020
|
|
Filing for new products
|
|
1
|
570
|
May 1, 2020
|
|
How to convert obsolete version BPR to live
|
|
1
|
608
|
May 1, 2020
|
|
Qualification of Cold Storage facility
|
|
1
|
605
|
April 28, 2020
|
|
Lay out of Production Area
|
|
1
|
489
|
April 28, 2020
|
|
Non Compliance Report/Supplier Corrective action Reports
|
|
1
|
642
|
April 28, 2020
|
|
Multiple Batches
|
|
10
|
683
|
April 20, 2020
|
|
Inprocess checking in sterile area
|
|
1
|
721
|
April 13, 2020
|
|
Copy of website content
|
|
0
|
826
|
April 11, 2020
|
|
How to handle controlled API or narcotic API
|
|
1
|
624
|
April 8, 2020
|
|
Document Retention period
|
|
7
|
2282
|
April 8, 2020
|
|
Primary packing supplier change and Stability study requirement
|
|
1
|
1500
|
March 30, 2020
|
|
Calculation on anhydrous basis
|
|
5
|
35718
|
March 24, 2020
|
|
Actual weight and conventional mass
|
|
3
|
562
|
March 20, 2020
|
|
Stability calculation
|
|
2
|
964
|
March 20, 2020
|
|
How to store narcotic substances
|
|
1
|
554
|
March 17, 2020
|
|
Stand alone CAPA
|
|
3
|
4016
|
March 13, 2020
|
|
Incidents & Deviations
|
|
1
|
624
|
March 4, 2020
|
|
How can prepare the EQ OQ PQ Protocols for pulverizer equipment
|
|
1
|
1314
|
February 29, 2020
|
|
Qus. For future
|
|
0
|
445
|
February 26, 2020
|