|
Hold time study for inprocess and bulk products
|
|
2
|
233
|
May 8, 2020
|
|
GMP quality system for a new facility
|
|
4
|
172
|
May 8, 2020
|
|
Diclofenac sodium tablet
|
|
4
|
310
|
May 7, 2020
|
|
Stability sample in first b
|
|
4
|
330
|
May 5, 2020
|
|
Process vlidation
|
|
8
|
561
|
May 5, 2020
|
|
Drug and cosmotic rule
|
|
1
|
106
|
May 5, 2020
|
|
Recommissioning of equipment
|
|
4
|
227
|
May 3, 2020
|
|
Balance qualification
|
|
3
|
443
|
May 2, 2020
|
|
Bioburden analysis
|
|
2
|
245
|
May 1, 2020
|
|
IPQA During Production
|
|
2
|
227
|
May 1, 2020
|
|
PH of the resulting solutions
|
|
2
|
242
|
May 1, 2020
|
|
Drug substance storage condition
|
|
2
|
221
|
May 1, 2020
|
|
cGMP Related doubts
|
|
2
|
300
|
May 1, 2020
|
|
Continual process verification
|
|
2
|
192
|
May 1, 2020
|
|
SOP FOR GOOD DISTRIBUTION PRACTICES
|
|
2
|
241
|
May 1, 2020
|
|
Packing material Shade card
|
|
3
|
233
|
May 1, 2020
|
|
Filing for new products
|
|
2
|
223
|
May 1, 2020
|
|
How to convert obsolete version BPR to live
|
|
2
|
115
|
May 1, 2020
|
|
Hold time study analysis
|
|
5
|
206
|
April 30, 2020
|
|
Hold time study
|
|
5
|
208
|
April 30, 2020
|
|
Qualification of Cold Storage facility
|
|
2
|
83
|
April 28, 2020
|
|
Lay out of Production Area
|
|
2
|
115
|
April 28, 2020
|
|
Non Compliance Report/Supplier Corrective action Reports
|
|
2
|
72
|
April 28, 2020
|
|
Multiple Batches
|
|
11
|
144
|
April 20, 2020
|
|
Inprocess checking in sterile area
|
|
2
|
136
|
April 13, 2020
|
|
Copy of website content
|
|
1
|
66
|
April 11, 2020
|
|
How to handle controlled API or narcotic API
|
|
2
|
249
|
April 8, 2020
|
|
Document Retention period
|
|
8
|
221
|
April 8, 2020
|
|
Primary packing supplier change and Stability study requirement
|
|
2
|
132
|
March 30, 2020
|
|
Calculation on anhydrous basis
|
|
6
|
432
|
March 24, 2020
|
