1
关注
1121
浏览

Can the cybersecurity descriptiondocument be submitted within the software descriptiondocument?

您还未登录!暂时最多只可查看 1 条回答

登录! 还没有账号?去注册

ku1314520 一阶会员 用户来自于: 广东省深圳市
2023-09-17 22:16

The“Guidance for premarket review for medical devicescybersecurity”is applicable to the registration and applicationof Class I and Class Il medical device products with networkconnection function for electronic data exchange or remote controland storage medium for electronic data exchange.

The cybersecurity description document is independent of thesoftware description document and shall be submitted separately.

关于作者

问题动态

发布时间
2023-09-17 22:16
更新时间
2023-09-17 22:16
关注人数
1 人关注

相关问题

If separately registered, do theyhave to clarify the matching situation?
How does FDA use the term “backup” in § 211.68(b)?
how to describe the computer in the productregistration?
What is the meaning of “Unit Quantity”?
Do we need the control groupin the animal experiment?
If the Android APP is registered, isit necessary to be tested when adding iOS APP?
changingthe center thickness of soft contact lenses?
Is it necessary to associate EMC test report withelectrical safety test report?
How to choose the operation mode in EMC test?
API 20 C AUX和API Candida有何区别?

推荐内容

变更是否需要启动体考?规定审评时限60日包括现场核查吗?
试剂和配套仪器共同开展临床试验,是否可以使用同一套临床试验资料分别进行注册申报?
接触镜类产品萃取性能研究中测试样品如何选择?
YY 0286.1-2019中药液过滤器排气孔细菌截留性能评价方法如何选择?
产品型号名称是否可以通过文字变更进行更改?
针对肾功能衰竭患者的血液净化产品生物学评价应如何考虑?
体外辅助生殖用耗材(体外辅助生殖用液除外产品需要进行鼠胚试验吗?
临床检验设备变更需要提交临床评价资料,属于免临床试验的产品其临床评价路径有推荐吗,是否是同品种的进行对比分析即可?
在体外诊断试剂的临床试验中,如采用 Sanger测序法作为对比方法,应提供哪些资料?
2021年申报的首次注册项目,目前在补正材料过程中,是否需要按照新发布的《定量检测体外诊断试剂分析性能评估注册审查指导原则》的要求补正分析性能评估资料?