total
No | title | Writer | Date | Hit |
---|---|---|---|---|
3 | CMC Postapproval Manufacturing Changes for Specified Biological Products To Be Documented in Annual Reports Guidance for Industry | 관리자 | Date20.03.09 | Hit392 |
2 | WHO guidelines on nonclinical evaluation of vaccines | 관리자 | Date20.03.09 | Hit384 |
1 | FDA guideline for Environmental assessment IND approval | 관리자 | Date20.03.09 | Hit351 |