| 1 x | Clinical Evaluation Report: Review for Regulatory Professionals | € 308.00 |
| 1 x | GCP for Investigators: Ethics and Legal Processes for Medical Device Clinical Investigations | € 84.00 |
| 1 x | ISO 14155_课程1_范围 | € 143.00 |
| 1 x | test training for stg env | € 12.00 |
| 1 x | second video test | € 9.00 |
| 1 x | 临床试验的启动 | € 95.00 |
| 1 x | 临床试验关闭或终止 | € 66.00 |
| 1 x | US Safety Reporting Requirements during Pre-Market Clinical Trials | € 72.00 |
| 1 x | Duplicate of wmdos-34 | € 20.00 |
| 1 x | GCP for Investigators: Clinical Investigation Close out or Termination | € 66.00 |
临床试验关闭或终止
临床试验关闭或终止
本次课程阐述了在哪些情况下临床试验可能被暂停或提前终止以及涉及各方的角色。概述了关闭临床试验的主要相关活动，包括强制要求报告给申办方，伦理委员会，主管当局或FDA。
本次课程内容根据：
- ISO 14155:2020版：应用于人类受试者的医疗器械临床试验
- 赫尔辛基宣言
- 21 CFR 812：试验用器械豁免
- 21 CFR 50：人类受试者的保护
观看课程预告
2 modules
€ 66.00
Add to Cart