China Begins the Inspection Program for Medical Device Clinical Trial Sites - July, 2017
- 2020-02-15 06:47:02
CFDA GCP Inspection Notification on 2016-07-08
- 2020-02-15 06:48:47
Qualtech and Croma (Austria) are currently under GCP inspection by CFDA in Sichuan Clinical Trial Institutions. The latest information will be posted up-to-date!
More Qualtech Chinese New Year holiday breaks
- 2020-02-15 06:49:44
Qualtech will be celebrating the festival and sharing joy and valuable times with families and friends.
More Speech regarding regulatory registration in Taiwan and China in Tokyo- July 30, 2013
- 2020-02-15 08:52:37
Qualtech was invited by OMETA (Overseas Medical Eauipment Tech. Assistants) to give the speech of regulatory registration in Taiwan and China.
More CFDA approval of Class III implant by Qualtech
- 2020-02-15 09:11:48
Qualtech had successfully got second CFDA approval license of Class III implant product in the end of December, 2012.
More SINGAPORE: Cybersecurity Labelling Scheme for Medical Devices ( CLS(MD) Sandbox: Latest Updates and Calls for Medical Device Manufacturers
- 2024-06-19 09:35:10
The rise of connected medical devices has revolutionized healthcare, but it has also introduced new cybersecurity challenges. To address these concerns, Singapore has implemented the CLS(MD) scheme, a collaborative effort to enhance medical device cybersecurity.
This article explores the latest updates on the CLS(MD) Sandbox program, its background, key details, and how medical device manufacturers can benefit from participation.
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