Overview of Device Regulation – FDA 2017

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%)*

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