MedTech I.Q.

The Cutting Edge of Medical Technology Content, Community & Collaboration

Overview of Device Regulation – FDA 2017

Event Details

Overview of Device Regulation – FDA 2017

Time: April 20, 2017 at 8:30am to April 21, 2017 at 5:30pm
Location: San Diego, CA
Street: Four Points By Sheraton San Diego Downtown 1617 1st Avenue - San Diego, California, 92101 - United States
City/Town: San Diego, CA
Website or Map: http://www.globalcompliancepa…
Phone: 800-447-9407
Event Type: overview, of, device, regulation, , fda, 2017
Organized By: NetZealous DBA as GlobalCompliancePanel
Latest Activity: Mar 2

Export to Outlook or iCal (.ics)

Event Description

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.

Why should you attend :

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: San Diego, CA Date: April 20th & 21st, 2017 and Time: 8:30 AM to 5:30 PM

 

Venue: Four Points By Sheraton San Diego Downtown

Address:  1617 1st Avenue - San Diego, California, 92101 - United States

 

Price:

 

Register now and save $200. (Early Bird)

 

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

 

Until March 15, Early Bird Price: $1,295.00 from March 16 to April 18, 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 Overview of Device Regulation – FDA 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