| 54 |
EU Packaging Readability Guidelines |
2006-11-17 |
| 53 |
FDA-Guidance 신규,개정,폐기 목록_2006년 |
2006-11-13 |
| 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 |
