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This comprehensive resource covers product change evaluation, postmarket surveillance, audit/inspection compliance, and various other laws and regulations pertaining to maintaining a product on the market.
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
What will the FDA do in 2023? In this timely, lively and informative event, regulatory analysts from POLITICO's AgencyIQ will explain what regulatory professionals should anticipate in the year ahead based on emerging trends, known issues, regulations and guidance documents and more.
Attendees of this session will come away with a better understanding of what FDA is working on, why they're working on it, and the potential impact that future actions may have on their business.
All regulatory topics discussed during this event will be about or directly related to the pharmaceutical, biopharmaceutical, biotechnology, medical device, diagnostic and dietary supplement sectors.
Free
To help regulatory professionals to anticipate actions that FDA is likely to take in 2023; To understand the challenges that FDA and industry are facing from a regulatory perspective.
Intermediate: Content is designed based upon the assumption that individuals have basic knowledge of the topic(s) and/or demonstrated competence related to the topic(s). Higher-level concepts are introduced during lectures; exercises requiring synthesis and/or application of concepts are incorporated into the activity.
Regulatory intelligence and policy professionals; Regulatory strategy professionals; Regulatory professionals interested in being proactive in anticipating regulatory actions.
Speakers:
Alexander GaffneyPOLITICO's AgencyIQ
Laura DiAngeloPOLITICO's AgencyIQ
Kari OakesPOLITICO's AgencyIQ
RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation.
All cancellation requests must be submitted in writing to raps@raps.org. RAPS is unable to accept cancellations by phone.
To transfer a registration, email raps@raps.org with the event title, name of the original registrant and the contact information for the new attendee.
For additional hands-on support, you can also connect with RAPS support 30 min prior to the workshop: https://www.raps.org/website/virtual-event-helpFor account support, contact the RAPS Support Center: +1 301 770 2920, ext. 200 (8:30 am–5:30 pm EST, Monday–Friday) or email support@raps.org.