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Education & Training

RAPS is committed to supporting the lifelong learning of regulatory professionals. RAPS’ educational resources and activities support the overall RAPS mission and the organization’s core values. RAPS is continually assessing the needs of regulatory professionals globally, and working with subject matter experts to develop and offer new, fair-balanced, evidence-based resources that will enable them to increase their knowledge, competence and performance.

Featured Program

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Medical Device Submission and Compliance Strategies for the US Market

13–14 March 2014
Rockville, MD

Featuring an expert panel of industry professionals and US Food and Drug Administration (FDA) regulators, this RAPS workshop will provide critical information on navigating the medical device submission process and creating compliance strategies for products for the US market. Attendees will get step-by-step instructions on how to effectively communicate with FDA and explore examples that will provide unique insight into the perspectives of both FDA and industry. Emphasis will be placed on audit inspections and premarket and postmarket compliance.

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Registration Details

RAC Points: 12

Advance Registration Deadline: 6 March 2014

On-site Registration Available: No
Please note that capacity for this program is limited. RAPS encourages participants to register early to confirm participation.

Cancellation Deadline: 14 February 2014

Questions? Call RAPS Solutions Center at +1 301 770 2920, ext. 200, or email raps@raps.org.

At a Glance

Meeting Location:
USP Meeting Center
12601 Twinbrook Parkway
Rockville, MD 20852
» Discover Rockville, MD

Registration Fees:
Members: $1,295.00
Nonmember: $1,520.00

» Register today
» Registration Form (PDF) - for registration by mail or fax.

Advance registration (online, mail and fax) will be accepted until 6 March unless capacity is reached for the meeting; after 1 September, please contact RAPS Solutions Center for registration options.