5 Things the Medical Device Industry Should Expect in 2017 (And How You Can Prepare)

What should the medical device industry expect in 2017?

Great question.

With all the new and proposed regulations in the past year, there is one thing you can bet on in 2017, change.

From the new EU MDR and IVDR, to the new version of ISO 13485:2016, to the increased focus on risk management by regulatory bodies across the globe, you will need to begin preparing for it all.

In this free 60 minute webinar, Jon Speer, an 18+ year medical device industry veteran and founder & VP QA/RA at greenlight.guru will be sharing some of his insights and observations for the upcoming year based on data and trends.

Join this webinar to stay one step ahead of the competition and learn how you can begin preparing for all the changes in store for 2017.

Specifically you will learn:

- Expected changes coming at FDA (and how they affect you)

- Quality inspection areas of concern

- Steps you can be taking to prepare for the transition to ISO 13485:2016

- What to expect when it comes to the new EU MDR & IVDR

- Tips on what to expect when putting together your FDA regulatory submission

Who Should Attend:

• Medical Device Executives
• Quality Assurance and Quality Control
• Regulatory Affairs and Compliance
• Manufacturing
• Supplier Management
• Internal, External and Quality Auditors
• Document Control
• Production
• Operations
• Suppliers to the Medical Device Industry
• R&D / Product Development

About greenlight guru

Greenlight Guru is the only Quality Management Software designed exclusively for medical device companies allowing them to bring safer devices to market faster while reducing risk and ensuring compliance. Click here to learn more about our software + services.