2023-10-17

Medical device industry set off a wave of mergers and acquisitions

M & A is a high-frequency word in the medical device industry in recent years. So far this year, the entire medical device industry has announced new deals at an alarming rate. According to Ernst & Young data, the medical device industry generated 33 M & A transactions in the first half of this year alone, which has exceeded the record for the whole of 2020. It is worth noting that in the global wave of medical device mergers and acquisitions, China's enterprises are very active.

2023-10-17

The theme of the 2021 Drug Digital Intelligence Development Conference "Building a New Pattern of Social Co-governance with Credit" was brilliant.

On September 28, 2021, the "2021 Drug Digital Intelligence Development Conference Building a New Pattern of Social Co-governance with Credit" hosted by the Information Center of the State Drug Administration (China Food and Drug Regulatory Data Center) was successfully held in Hefei, Anhui. More than 200 leaders from the local drug regulatory system, experts from the pharmaceutical industry and business representatives gathered together to talk about credit supervision.

2023-10-17

Medical device industry ushered in the "golden development period"

The national policy environment is conducive to the development of the industry. From 2017 to 2018, various policies were intensively introduced, and the 19th National Congress of the Communist Party of China included the "Healthy China Strategy" in the report; the review and approval of innovative medical devices accelerated, and the pilot of the registrant system continued to advance. The huge favorable policies and a good regulatory environment made the industry feel the arrival of the "good era.

2023-10-17

Top 10 Trends of Global Medical Device Industry in 2022

The European Union Medical Device Regulation (EU MDR) has entered the first full-year implementation phase. IVDR (In Vitro Diagnostic Medical Device Regulation) will be formally implemented from May 2022. Although the transition time has been extended, the equipment to be evaluated must be reviewed after the implementation of IVDR, and a series of problems still exist. Prior to the new device classification standard issued by IVDR, only about 20% of in vitro diagnostic devices (IVDs) required mandatory conformity assessment by designated agencies, and now this ratio has increased to about 80%.

2023-10-17

The advantages and application of vest type sputum machine

Vest sputum machine part of the use of comfortable and soft material, the patient's skin will not cause irritation, very comfortable to wear.