Process revalidation
|
|
0
|
154
|
June 12, 2025
|
Cleaning validation
|
|
0
|
114
|
May 18, 2025
|
Standard operating procedures
|
|
2
|
72
|
May 13, 2025
|
Annual quality review
|
|
4
|
78
|
May 8, 2025
|
API Shipments-lab sample
|
|
4
|
83
|
April 24, 2025
|
Temperature excursion study
|
|
1
|
695
|
March 2, 2025
|
Process Validation
|
|
4
|
181
|
February 28, 2025
|
Deviation or Incidence?
|
|
2
|
252
|
January 5, 2025
|
Can we use material after sterilization reset temperature in autoclave cycle?
|
|
3
|
99
|
December 24, 2024
|
Should this be a deviation? Why or why not
|
|
2
|
132
|
December 24, 2024
|
Need of change control for new facility
|
|
3
|
196
|
November 27, 2024
|
Process validation
|
|
3
|
200
|
November 27, 2024
|
Specimen signature
|
|
4
|
780
|
November 27, 2024
|
Criteria and selection of Sampling location and no of samples for cleaning validation in isolator for Onco products
|
|
1
|
520
|
November 27, 2024
|
Annexure of SOP
|
|
2
|
126
|
November 26, 2024
|
Was data integrity breached?
|
|
4
|
171
|
October 17, 2024
|
Risk analysis for other machine use use for capsule filling
|
|
1
|
984
|
October 14, 2024
|
Stability Study
|
|
0
|
256
|
October 9, 2024
|
What is the latest who gmp guidance on raw material sampling approach
|
|
2
|
433
|
September 16, 2024
|
A Harmonized Lable for storage condition of API shipments
|
|
1
|
248
|
September 2, 2024
|
Cleaning validation
|
|
1
|
625
|
August 14, 2024
|
Supply chain of finished product
|
|
3
|
859
|
July 30, 2024
|
Risk Assessment on HPLC Calibration frequency
|
|
0
|
396
|
July 29, 2024
|
Stamping of 'Uncontrolled copy' stamp on documents submission to DCA/CDSCO
|
|
1
|
414
|
July 1, 2024
|
Product Quality Review (PQR)
|
|
0
|
614
|
July 2, 2024
|
Raw Materials_Retesting_Extension of Shelf life
|
|
6
|
3131
|
June 11, 2024
|
In process control
|
|
0
|
501
|
June 9, 2024
|
Standard batch size
|
|
5
|
1184
|
June 2, 2024
|
Change over clearance
|
|
2
|
479
|
June 2, 2024
|
Internal audit evaluation
|
|
2
|
464
|
June 2, 2024
|