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

More Meetings

Medical Device Submission & Compliance Strategies for the US Market

5–7 March 2012
Rockville, MD

Learn to navigate the medical device submission process and manage compliance efforts for products in the US market. Hear directly from an expert panel of industry professionals and US Food and Drug Administration (FDA) regulators.
LEARN MORE

Registration Details

Discounted Registration Deadline: 6 February 2012

Advance Registration Deadline: 27 February 2012

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: 6 February 2012

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

At a Glance

Meeting Location:
RAPS Training Center

Hotel Information:
Suggested Hotels.

Will this meeting be recorded?: No

How do I obtain a Certificate of Attendance?
Submit your request onsite to the RAPS Education Program Manager or send a request to education@raps.org after the workshop.

RAC Points: 12

Registration Fees:
Members: $1,195.00
Non member: $1,420.00

» Register today