Global Network and Community

Regulatory Exchange

Expand your network and find solutions by collaborating with other regulatory professionals in this online community

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Membership for Individuals

Join more than 12,000 members from more than 60 countries to share knowledge and solutions

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Membership for Organizations

Give your regulatory team access to the resources they need to stay informed and meet with success

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Chapters

Connect with your local colleagues and build relationships that will last your entire career

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Event Calendar

What's coming up? Find an event near you

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International Community

Local or global—RAPS has you covered

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Social Media

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Industry Events

Non-RAPS professional development opportunities

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Regulatory Resource Directory

Consultancy and solutions from companies outside of RAPS

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Local or global—RAPS has you covered with offices in Washington, DC, Shanghai and Singapore. There are RAPS chapters in Canada, Switzerland, Taiwan and throughout the United States, and local networks in Australia, Belgium, Brazil, Germany, India, Mexico, The Netherlands, Poland and Singapore.

 

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Upcoming Global and Virtual Events

03
May
Virtual Program: Understand the New EU Medical Device/IVD Regulations 03 - 24 May 2017, Online, Webcast

This four-week virtual program draws together industry experts and leading notified bodies who have been closely following the evolution of the proposed regulations, anticipating the final texts, developing positions on what will be required by the regulations, and understanding the impact on manufacturers, devices and systems both new and legacy.

04
May
RAPS Roadshow: Examining the New European Medical Device Regulations 04 - 04 May 2017, München, Germany, Face-to-Face

Please join regulatory professionals in your region for the first Regulatory Affairs Professionals Society (RAPS) Roadshow in Europe. This half-day event will feature RAPS’ executive director Paul Brooks, a recognized expert on medical device regulation. His presentation will address the key changes introduced by the new European Medical Device Regulation (MDR) including the expanded scope of the regulation, and changes in classification and conformity assessment.

09
May
RAPS New York/New Jersey Chapter: First Amendment Considerations for Off-Label and Healthcare Economic Information 09 - 09 May 2017, New York, NY, Chapter Event

This presentation is intended to familiarize regulatory professionals with new draft guidances; contextualize the First Amendment debate; explore the definition of “intended use;” and provide a working understanding of FDA’s current thinking about on-label vs. off-label communications and the appropriate sharing of healthcare economic information.

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