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FDA reeased a guidance dosument on design considerations and pre-market submission recomenndations for interoperable medical devices and herewith puts an emphasis on the rising improtance of connected medical devices for the health system.

A summary of the event taking place May 11 and 12 in the Otto Bock Science Center in Berlin. Markus Fleckenstein‌

Regulatory Considerations in the Design and Manufacturing of Implantable 3D-Printed Medical Devices Read more...

FDA How 3D CAD and Printing are Paving Way for Personalized Medicine Read more...

LinkedIn Article - Mastering Requirements and Validation for Medical Devices Read more...

LiveWorx - Proposed Agenda for Healthcare & Medical Device Industry Read more...

2017 Medical Devices Manufacturers Software Selection Guide | PTC Read more...

Medical Devices: Making The Right Choice – Achieve The Case For Quality Webcast Replay | PTC Read more...

PLM for Medical Device Manufacturers | PTC Read more...

Accelerating Medical Device Innovation While Mastering the FDA Case for Quality – The Vital Role of PLMWe live in an age where innovation is driven by Digital Transformation. Medical Device Companies are facing the unique challenge of remaining competitive in an environment where Read more...