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Unique Device Identifier Requirements for Combination Products-2025/6/25
2025-06-27查看详情 > -
Conducting Remote Regulatory Assessments Questions and Answers-2025/6/24
2025-06-27查看详情 > -
Q1 Stability Testing of Drug Substances and Drug Products-2025/6/23
2025-06-27查看详情 > -
Post-Warning Letter Meetings Under GDUFA-2025/6/20
2025-06-20查看详情 > -
ANDAs: Pre-Submission Facility Correspondence Related to Prioritized Generic Drug Submissions-2025/6/16
2025-06-16查看详情 > -
M11 Technical Specification: Clinical Electronic Structured Harmonised Protocol-2025/6/6
2025-06-06查看详情 > -
Hernia Mesh – Package Labeling Recommendations-2025/6/6
2025-06-06查看详情 > -
M11 Template: Clinical Electronic Structured Harmonised Protocol (CeSHarP)-2205/6/5
2025-06-06查看详情 > -
Transfer of a Premarket Notification (510(k)) Clearance – Questions and Answers-2025/6/5
2025-06-06查看详情 > -
CVM GFI #287 - Raw Data for Safety and Effectiveness Studies-2025/6/4
2025-06-06查看详情 >
