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Half-day, full-day or multi-day. Expand your regulatory knowledge by learning directly from the experts. Participate in live, online presentations to interact with the presenter(s) and fellow attendees without traveling. Expert-led presentations are delivered virtually to participants as they view the PowerPoint slides and listen to the presentation over the internet or by dialing in.  Get your questions answered during Q&A by regulatory experts and industry representatives who can clarify and elaborate specific areas of their regulatory expertise. These programs can last 5 hours over one day or consist of shorter modules over 1-2 weeks. You can expect four or more presentations per Lecture Series.

Once you register for a live event, you have 12 months of access to the on-demand recording in the RAPS Learning Portal. Presentation slides will be available to download, along with any additional handouts from presenters. Upon completion of the event, you can earn RAC credit for those looking to recertify. 

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Event Highlight

Advancing and Enabling Regulatory Science to Impact Policy at CDRH: The AIMBE FDA Scholars Program

In this on-demand program, the American Institute for Medical and Biological Engineering (AIMBE) Scholars share what was required to gain this prestigious role and how relationships with the FDA staff have affected their futures in the medical device industry positively. 

PURCHASE

On-Demand Library

RAPS webcasts and virtual events cover the trends and tools to help you maximize your regulatory efforts. Our on-demand library provides you with access to stream past webcasts and virtual events for 12 months. You can also download the presentation slides and handouts from the RAPS Learning Portal. Upon completion of the event, you can earn RAC credit for those looking to recertify. 

 

US Regulation of Advertising, Promotion and Labeling for Drugs

US Regulation of Advertising, Promotion and Labeling for Medical Devices

Developing and Sustaining Quality Management Systems in Compliance with Pharma Industry Standards
 

Email Submissions

Have an Idea or Proposal for a Future Virtual Event?
To submit a topic idea or proposal for a virtual event, complete the following form:

Policies

Online registration will close at 11:59 PM ET the night prior to the webcast or virtual event.

Written cancellations received by 11:59 PM ET five business days prior to the virtual event will be refunded the registration fee minus a 20% administrative fee.

All you need to participate is internet access and a telephone connection. Expert presenters virtually deliver their presentation, while participants simultaneously view the PowerPoint slides on their own computers. Audio is available via the internet as well as by dialing-in. During the Q&A, participants have the opportunity to have their questions answered by regulatory experts and industry representatives who can clarify and elaborate on specific areas of their regulatory expertise.

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