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2017

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Manufacturing

European Commission Provides Important Guidance on Qualification and Classification of Software Under New Medical Devices Regulations

Data Matters

NOVEMBER 1, 2019

The Guidance seeks to provide clarification to medical software manufacturers with respect to (i) when software is considered a device (qualification) and (ii) what risk category the device falls into (classification). This could have a significant impact for many software manufacturers. digitized patient images. Modular approach.

Manufacturing

Manufacturing Marketing Risk IT

China’s First Data Protection Measures Lifting Its Veils

HL Chronicle of Data Protection

JUNE 13, 2019

The draft Data Security Measures appear to mainly target the data processing activities of “network operators,” which under these draft measures has the same definition as is used in the Cyber Security Law , namely, including the owner or administrator of a network or a network service provider. credit information companies).

Personal data

Personal data IT Data collection Compliance

European Commission Provides Important Guidance on Qualification and Classification of Software Under New Medical Devices Regulations

China’s First Data Protection Measures Lifting Its Veils

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