 |
EU GMP - Annex 1 Revision - Second Draft 발표 |
관리자 |
2020-02-26 |
1030 |
| 31 |
2018년 FDA Warning Letter - Data Integrity 관련 |
관리자 |
2019-08-13 |
1023 |
| 30 |
Peoples in Cleanrooms |
관리자 |
2019-07-01 |
367 |
| 29 |
How to write an effective SOP |
관리자 |
2019-06-10 |
382 |
| 28 |
How Does a Laboratory Autoclave Work? |
관리자 |
2019-06-04 |
353 |
| 27 |
Smoke Studies |
관리자 |
2019-05-28 |
410 |
| 26 |
Common Causes for Failure of a Bowie-Dick Test |
관리자 |
2019-05-24 |
547 |
| 25 |
Choose a Steam Source for Your Autoclave |
관리자 |
2019-05-24 |
330 |
| 24 |
Steam Sterilization Cycles |
관리자 |
2019-05-23 |
392 |
| 23 |
Qualification of Identical Pieces of Equipment |
관리자 |
2019-05-22 |
384 |
| 22 |
Responding To Regulatory Inspection Observations |
관리자 |
2019-05-22 |
314 |
| 21 |
Do and Don't during FDA Inspection |
관리자 |
2019-05-22 |
376 |
| 20 |
How To Write An Effective Validation Master Plan |
관리자 |
2019-05-22 |
421 |
| 19 |
Kill the Bioburden, Not the Biological Indicator |
관리자 |
2019-05-20 |
353 |
| 18 |
Understanding Overkill Sterilization |
관리자 |
2019-05-20 |
374 |
| 17 |
Contaminated LVPs and the Origins of Validation |
관리자 |
2019-05-20 |
361 |
| 16 |
Myths, Fantasies, and Rumors about Water System |
관리자 |
2019-05-20 |
367 |
| 15 |
Revisiting the Moist Heat Sterilization Myths |
관리자 |
2019-05-20 |
376 |
| 14 |
Ambient, Room Temperature, Cold - what is what? |
관리자 |
2019-05-15 |
361 |
| 13 |
Air and Contamination Control (by Tim Sandle) |
관리자 |
2019-05-14 |
375 |
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