All news with the tag "Medical%20Devices"

In light of the COVID-19 pandemic and the current lockdown, India's Central Drugs Standard Control Organization (CDSCO) has announced to issue import licences for medical devices and in-vitro diagnostic (IVD) kits, even if the required notarised / apostilled documents cannot be presented at the moment.

The Indian Ministry of Health and Family Welfare has announced that all medical devices in India will be notified as drugs and regulated under the Drugs and Cosmetics Act of 1940 effective 1 April 2020.

On 24 September 2019, German Federal Ministry for Economic Affairs and Energy (BMWi) and the National Medical Products Administration of China (NMPA) held a joint workshop on current regulatory topics for medical devices in Suzhou, China. As part of the Sino-German cooperation on Quality Infrastructure, the event provided a platform for dialogue and direct exchange between German authorities and industry representatives with Chinese regulators.

On 23 October 2015, the General Administration for Quality Supervision, Inspection and Quarantine (AQSIQ) and the Federal Ministry for Economic Affairs and Energy (BMWi) jointly hosted a workshop in Beijing on import inspection requirements for medical devices.