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 | Hit470 |
| 2 | WHO guidelines on nonclinical evaluation of vaccines | 관리자 | Date20.03.09 | Hit463 |
| 1 | FDA guideline for Environmental assessment IND approval | 관리자 | Date20.03.09 | Hit411 |