中国国际医疗器械设计与制造技术展览会(Medtec China)2021

Dedicated to design & manufacturing for medical device

August 31-September 2 2022 | SWEECC H1&H2

  • Medtec China 2022 is now open for visitor registration, helping medical device manufacturers in Medtech sourcing and Supply Chain stabilization

    Medtec China 2022 officially open for visitor registration, helping medical device manufacturers in Medtech sourcing and Supply Chain stabilization. The exhibition will take place in Shanghai from August 31 to September 2 in Shanghai China.

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  • Manufacturing Needs to Build a Better Workforce

    The U.S. manufacturing industry is expected to have as many as 2.4 million vacant manufacturing jobs in the next five years – just in case you weren't already concerned about the manufacturing labor shortage.

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  • Recent Trends in Self-Administration Drug Delivery Systems

    Drug delivery is changing, and with that the patient experience has evolved. Now, Distance Care is maximizing diagnostic and therapeutic self-care outside of the hospital environment. Patients are no longer tethered to the nurse, clinic, or other healthcare professional/setting to receive a drug infusion or another treatment.

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  • Big Prospects for Medical Device Miniaturization

    Strides in medtech miniaturization have enabled surgeons to reach remote areas of the body and have also made healthcare more accessible through portable and wearable medical devices. But while much has been accomplished, there are still potential new gains. There are also challenges to overcome as medtech innovators continue to shrink the state of the art—but there are solutions.

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  • 5 Thoughts on Harmonization of Quality Regulation

    On Feb. 23, FDA published a proposed rule intended to harmonize its quality regulation requirements with the international consensus standard for medical devices manufacturers (ISO 13485:2016). The proposed rule is now open for public comments at www.Regulations.gov under docket number (FDA-2021-N-0507). The new rule would replace the Quality System Regulation (QSR), at 21 C.F.R. Part 820, with a newly named Quality Management System Regulation (QMSR).

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  • More Effective Medical Device Development

    The World Health Organization estimates that there are 2 million different kinds of medical devices on the world market today. When designing and developing highly complex medical devices, certain best practices should be kept in mind throughout the design and development process.

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