Process chain practical? And presented by experts! Knowledge of the high-tech stream of time
The Forum for Developers and Suppliers in Hall 8b G40
A practical presentation of the latest developments throughout the process chain. Expert talks focus on mechanical and electronic components, innovative materials, manufacturing processes, manufacturing services of all kinds, design and usability aspects and quality assurance. Further main topics are additive manufacturing, electronic and regulatory affairs. Power presentations on innovative new markets round off the exciting program. The COMPAMED SUPPLIER FORUM is organized by DeviceMed, the leading German-language trade magazine aimed at manufacturers of medical technology products.
Review 2019
Program of the COMPAMED SUPPLIERS FORUM by DeviceMed 2019
10:45 – 11:00 h Begrüßung und aktuelle Lage der Medizintechnikbranche Peter Reinhardt, Chefredakteur, Devicemed
11:00 – 11:30 h New test strategies for biocompatibility: Go for chemical characterization and in vitro testing of your medical device Anja Friedrich, Eurofins Medical Device Testing
11:30 – 12:00 h From tech to hightech to medtech: 5000 years of learning for medical technology from other technologies Daniel Pressl, Wild
12:00 – 12:30 h Packaging and product testing services Noel Gibbons, Steris Applied Sterilization Technologies
12:30 - 13:00 h The basic principles of chemical characterization including the upcoming changes David Moreels, Nelson Laboratories
13:00 - 14:30 h
Session: Additive Manufacturing
13:00 – 13:30 h Developments impacting the medical AM/3DP process Lauralyn McDaniel, ASME
13:30 – 14:00 How regulations help understanding materials to get from prototyping to 3D printing volume production Gabi Janssen, DSM Additive Manufacturing – Business Development Manager Healthcare & Dental
14:00 – 14:30 Develop your Product 4.0 with optimised part design in a smart factory Birgit Schliwa, Proto Labs Germany GmbH
14:30 – 15:00 h Powerful energy solutions for medical applications Johannes Durschang, Varta Microbattery
15:00 – 15:30 h Challenges and opportunities for the European medtech industry Cordula Rapp, Spectaris e.V.
15:30 – 16:00 h MDD 93/42/EEC Art. 11 (MDR Art. 52) vs. 12 (MDR Art. 22) - Gaining experience and approaching MDR David Thaler, Mednet
16:00 - 16:30 h Usability engineering and MDR - a how to Michael Engler, Benkana Interfaces
16:30 – 17:00 h From tech to hightech to medtech: 5000 years of learning for medical technology from other technologies Daniel Pressl, Wild
[Version: 18 November 2019, subject to changes]
Tuesday, 19 November 2019
11:00 – 11:30 h What to expect when you are not expecting… the FDA Lacey Chessor, Knoell Germany
11:30 – 12:00 h Sustainable ethylene oxide processing Richard Cowman, Steris Applied Sterilization Technologies
12:00 – 12:30 h A current update on ISO 10993: past and future changes Thor Rollins., Nelson Laboratories
12:30 - 13:00 h Gaining a competitive edge through user centred design and IEC62366 compliance Mark Costello, Synecco
13:00 - 14:30 h
Session: Electronics
13:00 – 13:30 h MDR – How electronic contract manufacturers can help medical device manufacturers ensure compliance with the new Regulation Mauro Di Chello, Valtronic
13:30 - 14:00 h Viele Disziplinen - eine Aufgabe: Wie Sie Übergaben in der Medizinprodukteentwicklung optimal gestalten Holger Frank, Mechatronics Dr.-Ing. Benjamin Franz, Custom Interactions
14:00 – 14:30 h Qualitätssicherung und Traceability beim Transport medizinischer Geräte Maximilian Junge, SMT ELEKTRONIK
14:30 h – 15:00 h Regulatory requirements for the development of medical device software Vera Naumburger, Knoell Germany
15:00 – 15:30 h Develop your Product 4.0 with optimised part design in a smart factory Birgit Schliwa, Proto Labs Germany GmbH
15:30 – 16:00 h Issue prevention and resolution for injection molded medical parts Thomas Bechtel, Milacron
16:00 – 17:00 h Xing Messelounge – Networking der Xing Ambassador Community Medizintechnik [Version: 11 November 2019, subject to changes]
Wednesday, 20 November 2019
11:00 – 11:30 h Improve product quality and operational efficiency with paperless processes Stephen Turnock, MasterControl
11:30 – 12:00 h Disruptive light source covering ultraviolet to mid-infrared wavelengths delivers unmatched radiance Bill Grube, Hamamatsu
12:00 – 12:30 h Zulassung von Medizinprodukten unter der MDR / Funk in der Medizintechnik Thomas Ring, TÜV Süd
12:30 – 13:00 h The effects of material properties on the ability to cold form and machine small medical components Dr. Peter Hale, Deringer-Ney
13:00 - 14:30
Session: Regulatory Affairs
13:00 – 13:30 h Regulatory affairs from the start up perspective – chances and challenges within the regulatory approval process of patient individualised implants Valentine Gesché, Peragraft
13:30 – 14:00 h Die nationale Ausgestaltung der MDR. Wodurch wird das MPG im Mai 2020 abgelöst? Dr. Christina Zimmer, BVMed - Bundesverband Medizintechnologie
14:00 – 14:30 h Medical device registration: good news from Brazil Diego Louzada, Knoell Germany
14:30 – 15:00 h Develop your Product 4.0 with optimised part design in a smart factory Birgit Schliwa, Proto Labs Germany GmbH
15:00 – 15:30 h Continuous innovation: The evolution of xenon medical lighting James Clements, Excelitas
15:30 – 16:00 h Wound prevention Concept Dr. Marc-Stephan Weiser, Covestro
16:00 – 16:30 h MDR on short notice - current state of play and assumptions Stefan Bolleininger, be-on-Quality
16:30 – 17:00 h Additive Manufacturing for medical devices: A versatile tool to support the whole product lifecycle Arnaud Toutain, Stratasys
[Version: 18 November 2019, subject to changes]
Thursday, 21 November 2019
11:00 – 11:30 h IVD Regulation: Hands-on strategies for your way into a new area Peggy Synwoldt., Knoell Germany
11:30 – 12:00 h Material selection for next generation medical implants Dr. Jochen Ulmer, Euroflex
12:00 – 12:30 h How to integrate usability documentation for FDA and IEC 62366 Kay Behrenbruch, Benkana Interfaces
12:30 - 13:00 h Piezoceramic sensors and transducers in the medical industry Richard Miles, CeramTec
13:00 - 14:30 h
Session: Additive Manufacturing
13:00 – 13:30 h Leak and flow testing of medical devices in the manufacturing process Dr. Joachim Lapsien, CETA Testsysteme
13:30 – 14:00 h Von Research & Development zur Serienproduktion - Additive Fertigung in der Medizintechnik Laura Kastenmayer, TRUMPF Laser- und Systemtechnik
14:00 – 14:30 h Reinvent medical devices with 3D printing Daniel Princ, Stratasys
14:30 – 15:00 h Sustainable Sterilization Technologies for medical Devices Hans Maijer, Steris Applied Sterilization Technologies
