GlobalCompliancePanel is a training source that delivers diverse, high quality regulatory & compliance trainings. These trainings are simple while being relevant and cost-effective while being convenient.

GlobalCompliancePanel imparts knowledge of best practices across a broad range of user-friendly mediums such as webinars, seminars, conferences and tailored, individualized consulting. These help organizations and professionals implement compliance programs that meet regulatory demands and put business processes in place.

GlobalCompliancePanel focuses primarily on providing extensive and quality training in these core areas and anything related to them:

  • Risk Management
  • Regulatory Compliances
  • Corporate Governance
  • Quality Management
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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 the MDR for Europe

Start Date : November 29, 2018
End Date : November 30, 2018
Time : 9:00 am to5:00 pm

Phone : 18004479407
Email : globalcompliancepanel@gmail.com

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





Who will benefit:


Personnel who want to know all aspects of the CE Mark, Technical File and Design Dossier and the impact from the new MDR for EU. Medical device professionals in areas of Quality and Regulatory Affairs, design, risk management, postmarket activities, R&D, and manufacturing, who work for manufacturers that market devices in the EU. Employees and personnel who will benefit include:



 


Agenda:


Day 1 Schedule




Lecture 1: 
Technical File/Design Dossier/CE Mark



Day 2 Schedule




Lecture 2: 
Technical File/Design Dossier/CE Mark





Lecture 3: 
Consulting Case Study Practice





Lecture 4: 
Case Study Practice



Best Practices and Trends




Lecture 5: 
Interactive Exercises and Discussions





Questions and Summary




Recap of Day 2 


 


Speaker:


David R. Dills


Global Regulatory Affairs & Compliance Consultant and President, NovaQual 



David R. Dills, Global Regulatory Affairs & Compliance Consultant, Interim President, currently provides global regulatory affairs, compliance and quality consultative services for early-stage and established Class I/II/III medical device, including combination products, In Vitro Diagnostics, nutraceuticals/supplements, cosmetics and biopharmaceutical manufacturers in multiple medical specialties and therapeutic areas on the global landscape, and has an accomplished record with more than 26 years of experience in the areas of Regulatory Affairs, Compliance and Quality Systems. He has been previously employed, with increasing responsibilities, by medical device manufacturers and consultancies, including a globally recognized CRO, and has worked directly with manufacturers engaged in compliance remediation activities and services involving consent decrees, CIA's, warning letters,483 observations, and customer generated compliance events. He prepares for and conducts QS and regulatory audits He is currently acting and interim President at NovaQual LLC.


 


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


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Registration Info

 

https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901864SEMINAR?meetings4docs-nov-seocall 555-5555 for more info...

Contact the Organizer

Organized by

Organized by globalcompliancepanel

NetZealous LLC - DBA GlobalCompliancePanel ,
161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA., https://www.trainhr.com

GlobalCompliancePanel is a training source that delivers diverse, high quality regulatory & compliance trainings. These trainings are simple while being relevant and cost-effective while being convenient.

GlobalCompliancePanel imparts knowledge of best practices across a broad range of user-friendly mediums such as webinars, seminars, conferences and tailored, individualized consulting. These help organizations and professionals implement compliance programs that meet regulatory demands and put business processes in place.

GlobalCompliancePanel focuses primarily on providing extensive and quality training in these core areas and anything related to them:

  • Risk Management
  • Regulatory Compliances
  • Corporate Governance
  • Quality Management
Tel: 18004479407
Email: globalcompliancepanel@gmail.com
Website: http://www.globalcompliancepanel.com


Event Categories: Health & Nutrition.




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