BASEL, SWITZERLAND
PUBLIC TRAINING
Learn about the new EU Medical Device Regulations and how it will impact your organization. The MDR has new risk classifications. Learn more about Quality Risk Management, including effective tools such as the FMEA and the Fault Tree Analysis.
One day Training Course: New EU MDR 2017/745
- Discuss new EU Medical Device Regulations
- Impact, Application, planning, and resources
- New Risk Classification Criteria
- Complete Gap Analysis
- Plan education and training for 2020 full execution
1 Day Course
REGISTER HERE!
Two Day Training Course: Quality Risk Management
- Reduce risk in systems and processes.
- Improve risk awareness.
- Identify risk measures.
- Properly apply Risk Management tools, like Fault Tree Analysis and FMEA.
2 Day Course
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Event in partnership with
“Greenlight Guru is the only quality management platform designed specifically for medical device companies. The platform helps companies get safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more. Greenlight Guru’s platform is used by thousands of users across the globe to push beyond baseline compliance achieving True Quality. For more information, visit http://www.greenlight.guru.”
View our other Open Enrollment locations for 2018 HERE!
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One 1 Day Course……………….$699
Early Registration available for individual courses! No code required!
(Click on registration link for current early bird pricing)
BOTH courses…………………….$1699
Exact venue TBD.
Fill out the form below, and a PathWise representative will get back to you with an on-site training !
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