|
How i reduce CIP time
|
|
1
|
32
|
May 24, 2022
|
|
Glove integrity
|
|
1
|
75
|
May 6, 2022
|
|
Personnel Qualification for clean room
|
|
1
|
214
|
September 25, 2021
|
|
SIP mapping of Machine
|
|
0
|
149
|
May 31, 2021
|
|
Aproach of bio-decon study
|
|
0
|
161
|
March 17, 2021
|
|
Sterilisation of parenterals
|
|
2
|
449
|
August 1, 2020
|
|
What is importance of differentional pressure in pharma
|
|
13
|
3364
|
December 8, 2019
|
|
Dry Powder Parenteral Future Growth
|
|
0
|
350
|
October 30, 2019
|
|
Dry Powder Parenteral (Contract Manufacturing) market growth and demand
|
|
0
|
336
|
October 24, 2019
|
|
LAF air velocity
|
|
5
|
1000
|
April 28, 2019
|
|
Biological products
|
|
0
|
432
|
June 2, 2018
|
|
Do we have guidelines for Fogging machine used in Clean room disinfection ..?
|
|
4
|
993
|
June 1, 2018
|
|
differential pressure
|
|
0
|
551
|
February 12, 2018
|
|
Fumigation procedure
|
|
6
|
2223
|
January 17, 2018
|
|
Sterilization of nebulizer solutions
|
|
0
|
472
|
September 26, 2017
|
|
Can we manufacture non-penicillin beta lactam in the same facility
|
|
3
|
1111
|
September 23, 2017
|
|
Sampling in sterile condition
|
|
2
|
687
|
July 24, 2017
|
|
PQ isolator sterility testing
|
|
0
|
671
|
March 19, 2017
|
|
Requirement of change rooms for ophthalmic/sterile plant
|
|
2
|
1127
|
March 13, 2017
|
|
Difference between 0.2 and 0.22 micron filters
|
|
1
|
3543
|
December 9, 2016
|
|
Why do we use terminal sterilization after blow fill seal production?
|
|
2
|
1017
|
August 25, 2016
|
|
Leachiability in parental preparation how it determin
|
|
0
|
847
|
July 2, 2016
|
|
Biosafety cabinet
|
|
2
|
1212
|
June 23, 2016
|
|
Media fill requirement
|
|
1
|
1331
|
June 15, 2016
|
