total
No | title | Writer | Date | Hit |
---|---|---|---|---|
13 | Biosafety Guidance for Working with Viral Vectors | 관리자 | Date22.08.16 | Hit229 |
12 | Guidance for Industry process validation | 관리자 | Date20.03.11 | Hit542 |
11 | Guidance for Industry CGMP guideline of Phase I Investigational drug | 관리자 | Date20.03.11 | Hit537 |
10 | Preclinical Assessment of Investigational Cellular and Gene Therapy Products | 관리자 | Date20.03.09 | Hit571 |
9 | vol6c_guidance on ERA_GMO | 관리자 | Date20.03.09 | Hit471 |
8 | Overview of comments on _Guideline on the quality, nonclinical and clinical aspects 4 of gene therapy medicinal products | 관리자 | Date20.03.09 | Hit373 |
7 | ICH guideline Q11 on development and manufacture of drug substances chemical entities and biotechnological biological entities | 관리자 | Date20.03.09 | Hit328 |
6 | GUIDANCE FOR INDUSTRY | 관리자 | Date20.03.09 | Hit328 |
5 | FDA guideline for Environmental assessment IND approval | 관리자 | Date20.03.09 | Hit330 |
4 | Drug Master Files Guidance for Industry | 관리자 | Date20.03.09 | Hit398 |