Hall 2 / C 2071
The laws, regulations and standards hang like a sword of Damocles over the heads of medtech companies, especially medtech start-ups. The topic of "overregulation" seems to have become a daily mantra. But do regulations really slow down innovation?
Hall 2 / E 2134
Laser welding of plastics, like any joining technique, has its own design rules to achieve good and reliable joints. Additionally to machines, ProByLas also offers support on the design of the plastic parts to weld in order to apply the laser process optimally.
Hall 2 / F 2185
Signer Titanium maintains the world's largest stock of thin titanium sheets with a thickness of 1 mm - 3 mm. Your perfect contact for titanium semi-finished products for the manufacture of bone plates.
Hall 2 / F 2187
Since May 26th 2021, the Medical Device Regulation is fully applicable. Hence, all processes related to design, industrialization, manufacturing, marketing and market surveillance have to be aligned with the quality management system which must be compatible with ISO 13485:2016 and/or USA QSR.
Hall 2 / F 2170
denovoSkin™ from CUTISS AG is on its way to becoming a revolutionary therapy for large skin defects (e.g. due to burns). The treatment is carried out with "personalised tissue". The production of such transplants on a large scale has now been achieved with denovoCast from CSEM.
Swiss Medtech Expo ist the trade fair for Europe's third- largest Medtech market. Leading suppliers, research and educational institutes as well as specialised service providers will be demonstrating their competencies.
The 4th Swiss Medtech Expo turns the spotlight onto twelve focus topics. They show visitors what topics they must address to successfully implement their Medtech projects – from boosting performance to small-volume production and quality assurance.
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