共 50 条
- [45] Changes in the Review Period of Drug Application and a Drug Lag from the FDA and the EMA: An Industry Survey in South Korea Between 2011 and 2020 Therapeutic Innovation & Regulatory Science, 2023, 57 : 552 - 560
- [46] Highly variable drugs: Observations from bioequivalence data submitted to the FDA for new generic drug applications AAPS JOURNAL, 2008, 10 (01): : 148 - 156
- [47] Highly Variable Drugs: Observations from Bioequivalence Data Submitted to the FDA for New Generic Drug Applications The AAPS Journal, 2008, 10 : 148 - 156
- [48] The economic consequences of US FDA new drug approvals: evidence from Taiwan pharmaceutical and biotech companies INNOVATION-ORGANIZATION & MANAGEMENT, 2021, 23 (03): : 354 - 374
- [49] FDA EXTENDS EDUCATIONAL PERIOD FOR NEW POLICY ON COMPOUNDING ANIMAL DRUGS FROM BULK DRUG SUBSTANCES JAVMA-JOURNAL OF THE AMERICAN VETERINARY MEDICAL ASSOCIATION, 2022, 260 (14): : 1772 - 1773