COMPAMED SUPPLIERS FORUM by DeviceMed

Process chain practical? And presented by experts! Knowledge of the high-tech stream of time

The Forum for Developers and Suppliers

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.

The Forum program at virtual.COMPAMED 2020

Experience a medical technology highlight in virtual form that can be accessed by anyone from anywhere - virtual.COMPAMED from vom 16 - 19 November 2020. And where you can still discover innovations, maintain contacts and stay up to date through knowledge transfer.

CONFERENCE AREA

Also at virtual.COMPAMED, there will be exciting lectures, discussion rounds, live pitches and much more from our forum and conference area to experience.

We will put together an interesting program for you with live and also pre-produced highlight contributions. And this during the entire 4-day period in two video streams:

an English stream daily from 10:00 to 16:00 o'clock
and
a German stream from 10 to 14 o'clock.

All contributions will be recorded and will be available on demand via COMPAMED.de also after virtual.COMPAMED.

Learn more at the Conference Area!

Organisation

Contact

Vogel Communications Group GmbH & Co. KG
Gustav-Stresemann-Ring 1

Phone: +49 (0)931 418 - 0
Fax: +49 (0)931 418 - 3200

www.devicemed.de

Review 2019

Program of the COMPAMED SUPPLIERS FORUM by DeviceMed 2019

Monday, 18 November 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]

Image: Speaker and audience at the COMPAMED SUPPLIERS FORUM by DeviceMed; Copyright: Messe Düsseldorf

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

[Version: 08 October 2019, subject to changes]

Agenda download of COMPAMED SUPPLIERS FORUM by IVAM 2019 [version: 19 Nov. 2019, subject to changes]

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