Events

New EU Medical Device Regulation | Updated Regulation 2018

Wednesday

Jun 27, 2018 – 9:00 AM - 6:00 PM

WILL BE ANNOUNCED SOON
Elk Grove Village, IL 60007 Map

More Info

Course "The New EU Medical Device regulation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Overview:
Regulation proposals of the European Commission Background
In 2012, the Commission adopted a package of measures on innovation in health. The package consisted of a Communication and two regulation proposals to revise existing legislation on general medical devices and in vitro diagnostic medical devices. In particular, the Directives on active implantable medical devices (90/385/EEC) and on medical devices (93/42/EEC) are intended to be replaced by a Regulation on medical devices, while the Directive on in-vitro diagnostic medical devices (98/79/EC) is intended to be replaced by a Regulation on the same subject. The revisions therefore affected all kinds of medical devices including in vitro diagnostic medical devices, from home-use items like sticking plasters, pregnancy tests and contact lenses, to X-ray machines, pacemakers, breast implants, hip replacements and HIV blood tests.
This Seminar will look at what to expect when the new regulation is implemented. Including: the transition period, Effect on Notified Bodies, Impact of the MDR on Quality Management Systems (QMS), technical documentation, clinical trial requirements, UDI and combination products.
Why you should attend:
Because the current Directive will be significantly altered and replaced by a Regulation which is legally binding on all Member States.
Areas Covered in the Session:
• The updated Regulation
• Implementation dates and transition
• Main changes and products affected
• Effect on medical device manufacturers
Who will benefit:
• Clinical Trial Managers
• Regulatory Affairs
• Medical Officers
Agenda:

Day 1 Schedule
________________________________________
Lecture 1 (90 Mins):
The new MDR main changes
• Main updates
• Transition periods
• Effect on medical device manufacturers
• Regulatory landscape
________________________________________
Lecture 2 (90 Mins):
Notified Bodies under the New MDR
• Effect on NBs
• When will NBs begin conformity assessment against the new Regulation?
• Main effect on medical device manufacturers
________________________________________
Lecture 3 (90 Mins):
Impact of the MDR on Quality Management Systems (QMS)
• When do I need to update my QMS?
• What main points need to be considered?
• Effect on medical device manufacturers
________________________________________
Lecture 4 (90 Mins):
Technical Documentation
• Class I and IIa devices
• Effect on class IIb devices
• Class III devices
CASE STUDY 1 - Including a walkthrough of expected outcomes for all case study exercises
Wrap up of day 1 & Q&A's
Day 2 Schedule
________________________________________
Lecture 1 (90 Mins):
Clinical aspects and testing
• Class I and IIa devices
• Effect on class IIb devices
• Class III devices
________________________________________
Lecture 2 (90 Mins):
Periodic Safety Update reports
• Content of PSUR
• Frequency
________________________________________
Lecture 3 (30 Mins):
Common Specification (CS)
Common Tech Specifications
________________________________________
Lecture 4 (90 Mins):
Combination Products
• Definitions
• Requirements
• Technical documentation
CASE STUDY 2 - Including a walkthrough of expected outcomes for all case study exercises
Wrap up of day 2 & Q&A's
Speaker
Salma Michor
PhD, MSc, MBA, CMgr, RAC

Salma Michor is founder and CEO of Michor Consulting Schweiz GmbH, serving such clients as Johnson & Johnson, Novartis, Shire, Pfizer and Colgate Palmolive. Previously, Michor worked for Chiesi-Torrex, Wyeth Whitehall Export Croma Pharma GmbH. She teaches regulatory affairs and clinical strategies at the University of Krems, Austria, and is an independent expert to the European Commission. She holds a PhD in thermal process engineering and an MSc in food and biotechnology from the University of Applied Life Sciences in Vienna, Austria; an MSc from King's College, University of London in food technology; and an MBA from Open University, and has earned the RAC (EU), CQA and is a Chartered manager.

Location: Chicago, IL Date: June 27th & 28th, 2018 and Time: 9:00 AM to 6:00 PM
Venue: WILL BE ANNOUNCED SOON
Price:
Price: $1,495.00 (Seminar Fee for One Delegate)
Register for 5 attendees Price: $4,485.00 $7,475.00 You Save: $2,990.00 (40%)*
Register for 10 attendees Price: $8,222.00 $14,950.00 You Save: $6,728.00 (45%)*
Sponsorship Program benefits for “New EU Medical Device Regulation | Updated Regulation 2018” 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=901615SEMINAR?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

Bring These Top Artists To Your City

Demand it! ®

and Never Miss a Show Again!

Powered by Eventful, a CBS Local Digital Media Business

 

More From 104.3 JAMS

Music NewsMusic News
MBX Four
Play.ItPlay.It

Listen Live