Register for "Sharpen Your Skills 2017" - Efficient Medical Device Development

 

Medical Devices Development - Sharpen your Skills 2017

May 30th, 2017 | Marriott Courtyard, Oerlikon

All options availableCompliant and Efficient Medical Device Development

An impossible combination? 

Join us to gather concrete and practical advise on how to meet trending medical device development challenges in 2017.

We have called on a group of experienced industry expert to share their latest best practices on how to eliminate problems with you.

Register now to reserve your seat!

We look forward to see you at this event. If you have any questions or information requests, please don't hesitate to This email address is being protected from spambots. You need JavaScript enabled to view it.


Key Learning Objectives

EU MDR: What really matters to manufacturers. And when.

What does the new EU MDR has in store for you? The 566 pages of the MDR contains a number of important changes for the medical device industry. Meet the challenges in time and in right order.

Hansjörg Riedwyl, CEO | ISS AG

Verification: yesterday, today & tomorrow

Test documentation takes up more than 50% of the total Design History File / Technical File. Time which could be better spent. Imagine 100% regression tests in a single day, for every release. Can it be made possible? Learn more in this session.

Tobias Müller, Managing Director | Progile GmbH

The seven sins of Clinical Evaluation Report writing

Regulatory requirements on clinical evaluation data has risen considerably during recent years. What are the best (and worst) practices in writing and updating state-of-the-art medical device CER:s?

Dr. Bruno Walter, Managing Director | Medical Minds

Digital Signatures = Quicker DHF Document Releases?

E-signatures boost document release efficiency according to business experts. Medical device development involves an awful lot of documents. So why should not everyone use e-signatures?  

Karl Larsson, Medical Device Documentation Expert | Aligned AG

 


Time and Place

  • Date: Tuesday May 30th
  • Time: 08:30 - 13:00
  • Place: Hotel Marriott Courtyard, Oerlikon Zürich

Presentations are held in german. Slides written in english.

Target audience

This event is aimed at medical device development professionals, project managers, QARA professionals, R&D personel and other industry professionals engaged in medical device development.

Registration

We are looking forward to see you at this seminar!

Registration Fee: 125 CHF

30% early bird discount for registration before May 10th

 


Location

Adress: Hotel Marriott Courtyard, Max-Bill-Platz 19, 8050 Zürich

 

 


About Aligned AG

Aligned AG provides Aligned Elements, a Medical Device ALM system that accelerates and ensures compliant Design Control documentation for medical devices. We assist our clients in developing regulatory compliant products within shorter time-frames, to lower costs and with higher confidence. 

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