2026. 9.1-9.3

Shanghai New InternationalExpo Center, N1-N4

Exhibition in

Days

Enhancing Manufacturing Efficiency with High-Performance Coatings

Medical device manufacturing is a highly regulated industry that demands precision and faces numerous challenges. Ensuring efficiency, compliance, and safety is crucial for maintaining the integrity of the manufacturing process and the quality of the final products.

Guest Editorial: The Power of One When Choosing Stent and Catheter Partners

As device designs become increasingly sophisticated, medtech companies are understandably seeking contract design and manufacturing partners that can accompany them on comprehensive product journeys — from initial concept to validation to large-scale manufacturing, and everything in between. This places a differentiating premium on partners with the ability to combine ideation and early-stage development with materials science and process technologies.

Designing Medical Devices with Intelligence

The medical device industry is experiencing rapid advancements in product design and prototyping as a result of new or improved manufacturing technologies. For example, “additive manufacturing has evolved from a novelty to a robust and mature method, enabling designers and product developers to create complex prototypes quickly and efficiently,” said Jim MacDonald, business development manager for Vaupell, a Constantine, Mich.-based contract manufacturer that provides engineering, design, and manufacturing services to the medical device industry.

The Critical Role of Supply Chain Visibility for Post-Market Surveillance

In recent years, medical device regulators have implemented stricter requirements for post market surveillance (PMS), as seen in frameworks like the EU Medical Device Regulation (MDR), the In Vitro Diagnostics Regulation (IVDR), and the UK’s Statutory Instrument (SI) coming into effect on June 16, 2025.

Thanks for your interested in 2026 Medtec,
the registration will be launche in April 2026.