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CE Mark Certification: Compile a CE Marking Technical File (or Design Dossier for Class III) containing evidence of compliance to the Medical Devices Directive (or the IVD/AIMD Directives) - Impact of

Event Details

CE Mark Certification: Compile a CE Marking Technical File (or Design Dossier for Class III) containing evidence of compliance to the Medical Devices Directive (or the IVD/AIMD Directives) - Impact of

Time: November 29, 2018 at 9am to November 30, 2018 at 5pm
Location: Hilton Zurich Airport
Street: Hohenbuhlstrasse 10, 8152 Opfikon-Glattbrugg, Switzerland. +41 44 828 50 50
City/Town: Zurich, Switzerland
Website or Map: https://www.globalcompliancep…
Phone: 18004479407
Event Type: seminar
Organized By: John Robinson
Latest Activity: Oct 30, 2018

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Event Description

Course "CE Mark Certification: Compile a CE Marking Technical File (or Design Dossier for Class III) containing evidence of compliance to the Medical Devices Directive (or the IVD/AIMD Directives) - Impact of the MDR for Europe" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Description:

Why you should attend

  • Introductions and overview of the EU Directives
  • Identify the EU Directives and standards applicable to your product
  • Comply with the implementation details and requirements of the EU MDR & IVDR
  • Design a new product, or evaluate an existing product, for conformity with these Directives and standards
  • Conduct and document a detailed Hazard Identification and Risk Assessment of your product
  • Complete the necessary Technical File and documentation required to meet EU legal requirements
  • Understand the relationship between CE Marking requirements
  • Determine exactly which materials need to be compiled
  • Completely review all existing documentation in support of meeting the applicable Essential Requirements of the Directive(s)
  • Evaluate and identify gaps or deficiencies in your documentation
  • Compile your EU Technical File or Design Dossier, with internal peer review
  • Determine applicable testing requirements and standards for your device

Location:  Zurich, Switzerland Date: November 29th & 30th, 2018 and Time: 9:00 AM to 5:00 PM

Venue:  Hilton Zurich Airport Hohenbuhlstrasse 10, 8152 Opfikon-Glattbrugg, Switzerland

 

Price:

Until October 20, Early Bird Price: $1,695.00 Price: $1,695.00 (Seminar Fee for One Delegate)

From October 21 to November 27, Regular Price: $1,895.00

Register for 5 attendees Price: $5,085.00 $8,475.00 You Save: $3,390.00 (40%)*

Register for 10 attendees Price: $9,322.00 $16,950.00 You Save: $7,628.00 (45%)*

 Register now and save $200. (Early Bird)

Sponsorship Program benefits for seminar

For More Information- https://www.globalcompliancepanel.com/control/sponsorship

Contact us today!

NetZealous LLC DBA GlobalCompliancePanel

john.robinson@globalcompliancepanel.com

Toll free: +1-800-447-9407

Phone: +1-510-584-9661

 Website: http://www.globalcompliancepanel.com

 

Registration Link -  https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901864SEMINAR?seo

Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/

Like us our Facebook page: https://www.facebook.com/TrainingsAtGlobalCompliancePanel/

Follow us on Twitter: https://twitter.com/GCPanel

 

 

 

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