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Overview of Device Regulation – FDA 2017

Embassy Suites Boston Logan Airport

Thursday, June 22, 2017

 

 

Course "Overview of Device Regulation - FDA" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This course provides a basic description of an FDA regulatory strategy for medical devices and explains the relationships between regulatory strategy and product development. It offers guidelines for developing successful strategies for medical devices, including definitions and classifications, elements of regulatory strategy, sources of regulatory intelligence, selection of development and product clearance/approval pathways. Location: Boston, MA Date: June 22nd & 23rd, 2017 and Time: 8:30 AM to 5:30 PM Venue: Embassy Suites Boston Logan Airport Address: Embassy Suites Boston Logan Airport 207 Porter Street Boston, MA 02128 Price: Register now and save $200. (Early Bird) Price: $1,295.00 (Seminar Fee for One Delegate) Until May 10, Early Bird Price: $1,295.00 From May 11 to June 20, 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: john.robinson@globalcompliancepanel.com Website: http://www.globalcompliancepanel.com Registration Link – http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900902SEMINAR?wooeb_June_2017_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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