| 52 |
PS 9004:Guide to GMP req for Pharm Pack. Material |
2006-10-12 |
| 51 |
Guidance for Industry "Investigating OOS" |
2006-10-12 |
| 50 |
Guidance for Industry |
2006-10-12 |
| 49 |
Guideline on Declaration of Herbal Substances and Herbal Preparations in Herbal Medicinal Products/T |
2006-10-05 |
| 48 |
Draft GUIDELINE ON VIRUS SAFETY EVALUATION OF BIOTECHNOLOGICAL INVESTIGATIONAL MEDICINAL PRODUCTS |
2006-10-05 |
| 47 |
ICH Quality Risk Management-History |
2006-09-21 |
| 46 |
EMEA - 식물생약 규격 Guideline에 대한 Comment |
2006-08-30 |
| 45 |
EMEA - 식물생약 품질 Guideline에 대한 Comment |
2006-08-30 |
| 44 |
EU Guideline_식물생약의 규격 |
2006-08-22 |
| 43 |
EU Guideline_식물생약의 품질 |
2006-08-22 |
