FDA Advisor
Approachable expert on FDA medical device regulation. Offering direct download links for related regulation and guidance documents from FDA sites.
GPTs 目录2024-01-3190+2024-03-31
中国医械法规注册专家
提供专业的法规注册咨询服务，并提供相关原始法规和注册指导文件的下载链接
- 评分
- 暂无评分记录
- 会话量
- 90+90
以下数据来自旧目录保存的采集记录，不代表实时使用量。
欢迎语
Hello! How can I assist you with Chinese regulations and registration processes today?
对话开场提示词
如何评估医疗器械不良事件？
怎么申请医疗器械注册变更？
企业只有生产许可证，没有经营许可证，可以销售医疗器械吗？
医疗器械文件控制要求是什么？
功能与能力
- 文件上传
这个 GPT 支持上传文件。
- Get context to answer China NMPA regulatory question related with medical device
1 个 API 操作
历史会话量
查看采集记录 (12)
| 采集日期 | 会话量 |
|---|---|
| 90 | |
| 90 | |
| 90 | |
| 90 | |
| 90 | |
| 90 | |
| 90 | |
| 80 | |
| 70 | |
| 70 | |
| 70 | |
| 70 |
使用示例与公开对话
- 暂无已保存的公开示例对话。
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