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Institutional Review Boards Frequently Asked Questions Guidance for Institutional Review Boards and Clinical Investigators-2025/2/5
2025-02-06查看详情 > -
Institutional Review Board (IRB) Written Procedures-2025/2/5
2025-02-06查看详情 > -
Recommendations to Reduce the Risk of Transmission of Disease Agents Associated with Sepsis by Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)-2025/1/31
2025-02-05查看详情 > -
Recommendations to Reduce the Risk of Transmission of Mycobacterium tuberculosis (Mtb) by Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)-2025/1/31
2025-02-05查看详情 > -
Bioanalytical Method Validation for Biomarkers-2025/1/21
2025-01-22查看详情 > -
Prevention and Treatment of Chemotherapy-Induced Peripheral Neuropathy: Developing Drug and Biological Products in Oncology-2025/1/17
2025-01-17查看详情 > -
Premarket Approval Application and Humanitarian Device Exemption Modular Review-2025/1/13
2025-01-14查看详情 > -
Obesity and Overweight: Developing Drugs and Biological Products for Weight Reduction-2025/1/7
2025-01-08查看详情 > -
Developing Drugs for Optical Imaging-2025/1/7
2025-01-08查看详情 > -
CVM GFI #187B Heritable Intentional Genomic Alterations in Animals: The Approval Process-2025/1/7
2025-01-07查看详情 >