MedTech I.Q.

The Cutting Edge of Medical Technology Content, Community & Collaboration

Medical Devices Industry and Risk Management 2017

Event Details

Medical Devices Industry and Risk Management 2017

Time: April 27, 2017 at 9am to April 28, 2017 at 6pm
Location: Seattle, WA
Street: Courtyard Seattle Sea-Tac Area 16038 West Valley Highway Tukwila Washington 98188 USA Phone: (425) 255-0300
City/Town: Seattle, WA
Website or Map: http://www.globalcompliancepa…
Phone: 800-447-9407
Event Type: medical, devices, industry, and, risk, management, 2017
Organized By: NetZealous DBA as GlobalCompliancePanel
Latest Activity: Mar 2

Export to Outlook or iCal (.ics)

Event Description

Overview:

Gaps, incorrect or incomplete implementation of software can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifecycle. Diligent, complete and correct implementation of risk management from the start of product development is therefore imperative. This course will introduce all necessary steps to design, implement and test critical medical device software in a regulatory compliant environment. Software risk management has to be embedded into the bigger scope of overall risk management. Therefore this course will additionally address the system level risk management and the resulting interfaces to software.

To comprehensively summarize all risk related activities and to demonstrate the safe properties of a device the 'Safety Case' or 'Assurance Case' document is a well-established method to collect all safety related information together in one place. This documentation will most likely become mandatory for all devices (currently only required for FDA infusion pump submissions). This course will introduce the basic concepts and content of safety assurance cases and will illustrate the usefulness for internal and external review of safety related information.

 

Location: Seattle, WADate: April 27th & 28th, 2017 and Time: 9:00 AM to 6:00 PM

 

Venue: Courtyard Seattle Sea-Tac Area

Address:  16038 West Valley Highway Tukwila Washington 98188 USA Phone: (425) 255-0300

 

Price:

 

Register now and save $200. (Early Bird)

 

Price: $1,295.00 (Seminar Fee for One Delegate)

 

Until March 20, Early Bird Price: $1,295.00 From March 21 to April 25, Regular Price: $1,495.00

 

Register for 5 attendees   Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*

 

Quick Contact:

NetZealous DBA as GlobalCompliancePanel

 

Phone: 1-800-447-9407

Fax: 302-288-6884

Email: support@globalcompliancepanel.com               

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

 

 

 

 

 

 

 

Comment Wall

Comment

RSVP for Medical Devices Industry and Risk Management 2017 to add comments!

Join MedTech I.Q.

Attending (1)

© 2017   Created by CC-Conrad Clyburn-MedForeSight.   Powered by

Badges  |  Report an Issue  |  Terms of Service