Industry News_News_ Blood and infusion warmer

2022-01-07

Raise the threshold again! The country releases new standards for Chinese medicine clinics

This series of questions have all been answered in the **new version of the standards for Chinese medicine clinics and Chinese medicine (general) clinics.

Which department does the pulmonary function tester use? What is the main test?

Which department does the pulmonary function tester use?

2022-01-07

Tighter supervision of medical devices after they are on the market

In 2019, the **Medical Device Adverse Event Monitoring Information System received a total of 396,300 effective suspicious medical device adverse event reports...

2022-01-07

Ministry of Education: Encourage medical schools to offer intensive care medicine courses

Recently, the website of the Ministry of Education released the "Reply to Recommendation No. 9874 of the Third Session of the Thirteenth National People's Congress"...

2022-01-07

Big change! National Health Commission: Will reduce the use of disposable medical devices

Recently, the National Health Commission issued the "Reply to Recommendation No. 9780 of the Third Session of the Thirteenth National People's Congress" (hereinafter referred to as the "Reply").

2022-01-07

A batch of medical devices were unqualified, and the Food and Drug Administration ordered a "recall for rectification"!

Jiangsu Provincial Food and Drug Administration, Siyu Research Institute, Medical Device Dealers Alliance

2022-01-07

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Raise the threshold again! The country releases new standards for Chinese medicine clinics

Which department does the pulmonary function tester use? What is the main test?

Tighter supervision of medical devices after they are on the market

Popular science posts | Contraindications for the use of commonly used life-saving drugs

Ministry of Education: Encourage medical schools to offer intensive care medicine courses

Big change! National Health Commission: Will reduce the use of disposable medical devices

A batch of medical devices were unqualified, and the Food and Drug Administration ordered a "recall for rectification"!