total
| No | title | Writer | Date | Hit |
|---|---|---|---|---|
| 13 | Biosafety Guidance for Working with Viral Vectors | 관리자 | Date22.08.16 | Hit335 |
| 12 | Guidance for Industry process validation | 관리자 | Date20.03.11 | Hit650 |
| 11 | Guidance for Industry CGMP guideline of Phase I Investigational drug | 관리자 | Date20.03.11 | Hit645 |
| 10 | Preclinical Assessment of Investigational Cellular and Gene Therapy Products | 관리자 | Date20.03.09 | Hit688 |
| 9 | vol6c_guidance on ERA_GMO | 관리자 | Date20.03.09 | Hit561 |
| 8 | Overview of comments on _Guideline on the quality, nonclinical and clinical aspects 4 of gene therapy medicinal products | 관리자 | Date20.03.09 | Hit472 |
| 7 | ICH guideline Q11 on development and manufacture of drug substances chemical entities and biotechnological biological entities | 관리자 | Date20.03.09 | Hit407 |
| 6 | GUIDANCE FOR INDUSTRY | 관리자 | Date20.03.09 | Hit408 |
| 5 | FDA guideline for Environmental assessment IND approval | 관리자 | Date20.03.09 | Hit409 |
| 4 | Drug Master Files Guidance for Industry | 관리자 | Date20.03.09 | Hit497 |