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Additional Registration Fee
Additional Registration Fee
Invitation Only
Invitation Only
Student Program
Student Program
Networking Opportunity
Networking Opportunity
RAPS Focus Area
RAPS Focus Area

Full Schedule

*Program and presenters subject to change. Please check back frequently for updates.

Full Schedule

  • Thursday, October 5, 2023
  • 12:00 AM – 5:00 PM EDT
    Wellness at RAPS Convergence
  • 6:30 AM – 3:00 PM EDT
    Registration Open
  • 6:30 AM – 4:30 PM EDT
    Speaker Ready Room Open
  • 6:30 AM – 7:00 PM EDT
    Luggage Check
  • 7:00 AM – 8:00 AM EDT
    Community Gathering & Continental Breakfast
  • 7:30 AM – 5:00 PM EDT
    RAPS Store Hours
  • 7:30 AM – 6:00 PM EDT
    Press Office Hours
  • 8:00 AM – 9:15 AM EDT
    Actionable Steps to Meeting Regulatory and Ethical Considerations in Clinical Trial Diversity
  • 8:00 AM – 9:15 AM EDT
    Considerations for Cannabidiol Product Development: The Regulatory Landscape and Safety Concerns.
  • 8:00 AM – 9:15 AM EDT
    Conversations That Matter - Interactions with Health Authorities: Medical Devices and IVDs
  • 8:00 AM – 9:15 AM EDT
    Device-Led Combination Products Regulatory Process – Hot Topics
  • 8:00 AM – 9:15 AM EDT
    How to Prepare Efficiently to Become IVDR-Compliant
  • 8:00 AM – 9:15 AM EDT
    Labeling - New
  • 8:00 AM – 9:15 AM EDT
    Lessons on the EU-Clinical Trials Regulation
  • 8:00 AM – 9:15 AM EDT
    Medical Device Cybersecurity: Planning a Global Strategy
  • 9:30 AM – 10:30 AM EDT
    Plenary Session: RAPS Patient-Centered Health Award Presentation and Panel Discussion: Progressing Patient-Centered Health Through Collaboration: A TransCelerate Multi-Stakeholder Panel
  • 10:30 AM – 11:00 AM EDT
    Coffee Break in the Exhibit Hall
  • 10:30 AM – 2:30 PM EDT
    Certification Lounge Hours
  • 10:30 AM – 2:30 PM EDT
    Exhibit Hall Hours
  • 10:30 AM – 2:30 PM EDT
    Headshot Lounge
  • 10:30 AM – 2:30 PM EDT
    Regulatory Cares Community Giveback
  • 10:30 AM – 2:30 PM EDT
    Student Capstone Poster Display: Survey of Clinical Trial Data of Immune Checkpoint Inhibitors – Avelumab and Cemiplimab
  • 10:30 AM – 2:30 PM EDT
    Student Capstone Poster Display: Clinical Paradigms in Immune Checkpoint Inhibitors: Pembrolizumab, Durvalumab, and Atezoliuzmab
  • 10:45 AM – 11:10 AM EDT
    Sponsored Presentation: Drive on the Regulatory Autobahn – Stretch Your Team with No Speed Limit
  • 10:45 AM – 11:10 AM EDT
    Sponsored Presentation: Risk Strategy & Risk Management for Medical Devices
  • 10:45 AM – 11:10 AM EDT
    Sponsored Presentation: What’s Next: The Evolution of Regulatory Submissions and Technology
  • 10:45 AM – 11:15 AM EDT
    Lessons on the EU-Clinical Trials Regulation
  • 10:45 AM – 11:15 AM EDT
    Solutions Circle - Continuing the Conversation: EU/MDR State of Play
  • 10:45 AM – 11:15 AM EDT
    Solutions Circle - Continuing the Conversation: Pediatric Drug Development:  Failure is not an Option
  • 10:45 AM – 11:15 AM EDT
    Solutions Circle - Continuing the Conversation: Regulatory Trends and Opportunities for Drug Delivery Combination Products
  • 11:00 AM – 11:30 AM EDT
    RAPS BOD Roundtable: Emerging Regulatory Trends
  • 11:15 AM – 11:40 AM EDT
    Sponsored Presentation: Crossing the eSTAR Chasm: how to transition to FDA’s Mandatory 510(k) eSTAR submission process
  • 11:15 AM – 11:40 AM EDT
    Sponsored Presentation: FDA Forecast: The Biggest Issues Facing the FDA in 2024
  • 11:15 AM – 12:00 PM EDT
    Student Mix 'n Mingle at Career Central
  • 11:15 AM – 11:40 PM EDT
    Sponsored Presentation: Optimizing CER and PMS document writing with technology and AI
  • 11:25 AM – 11:55 AM EDT
    How to Improve Regulatory Interactions by Practicing Impromptu Speeches
  • 11:25 AM – 11:55 AM EDT
    RAPS Store Stage: Writing for RAPS - All You Need to Know About Submitting Content for RAPS Publications
  • 11:25 AM – 11:55 AM EDT
    Solutions Circle - Continuing the Conversation: FDA Expectations for Digital Health Tools in Decentralized Clinical Trials
  • 11:25 AM – 11:55 AM EDT
    Solutions Circle - Continuing the Conversation: Get the 411 on 1.14
  • 11:25 AM – 11:55 AM EDT
    Trends on Orphan and Pediatric Regulatory Frameworks
  • 11:45 AM – 12:10 PM EDT
    Sponsored Presentation: Pharmaceuticals, Medical Devices, OTC’s and now Cosmetics – What to watch out for when managing a Product Recall
  • 11:45 AM – 12:10 PM EDT
    Sponsored Presentation: PMS Beyond Regulations
  • 11:45 AM – 12:10 PM EDT
    Sponsored Presentation: Sustainability: potential challenges and solutions for the MedTech industry, Notified Bodies and auditing organizations.
  • 11:45 AM – 12:15 PM EDT
    Career Central Stage: The RAPS Competency Framework and Tools: What is it and what's in it for me?
  • 11:45 AM – 12:15 PM EDT
    RAPS BOD Roundtable: The Futuristic Regulatory Professional
  • 12:00 PM – 1:30 PM EDT
    Networking Lunch in Exhibit Hall
  • 12:05 PM – 12:35 PM EDT
    Notified Bodies: IVDR implementation Ask me Anything
  • 12:05 PM – 12:35 PM EDT
    Solutions Circle - Continuing the Conversation: The eSTAR and I: Getting to Know the eSTAR Templates for FDA Submissions
  • 12:05 PM – 12:35 PM EDT
    The Journy to RAC!
  • 12:05 PM – 12:35 PM EDT
    Transparent, translucent, and opaque: how global health authorities make information publicly accessible
  • 12:15 PM – 12:40 PM EDT
    Sponsored Presentation: Managing regulatory change
  • 12:15 PM – 12:40 PM EDT
    Sponsored Presentation: The 80/20 Rule: How Digital Transformation & AI Are Changing Regulatory Intelligence
  • 12:15 PM – 12:40 PM EDT
    Sponsored Presentation: Unlocking the Power of Retrospective PMCF Studies for EU MDR Compliance
  • 12:30 PM – 1:00 PM EDT
    RAPS BOD Roundtable: I Am Regulatory
  • 12:45 PM – 1:10 PM EDT
    Sponsored Presentation: Global Medical Device UDI Status and How to Best Manage Diverse Compliance Rules
  • 12:45 PM – 1:10 PM EDT
    Sponsored Presentation: The Future of Change Management for Cloud-Based AI/ML Medical Software
  • 12:45 PM – 1:15 PM EDT
    Notified Bodies: IVDR implementation Ask me Anything
  • 12:45 PM – 1:15 PM EDT
    RAPS Store Stage: Meet the Authors - Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective
  • 12:45 PM – 1:15 PM EDT
    Using Situational Leadership to Manage yourself and others
  • 12:45 PM – 1:45 PM EDT
    RAPS Fellows Speed Mentoring at Career Central (Sign-up Required)
  • 1:15 PM – 1:45 PM EDT
    Career Central Stage: Get Certified in Regulatory Affairs: Get your RAC!
  • 2:00 PM – 3:00 PM EDT
    Biosimilar Regulatory Standards in the ICH Regions: Implications for Global Biosimilar Development
  • 2:00 PM – 3:00 PM EDT
    Health Authority Forum: Health Canada
  • 2:00 PM – 3:00 PM EDT
    Importance of Building Relationships with Health Authorities: Case Study for NDA Review of Orphan ProductXYZ
  • 2:00 PM – 3:00 PM EDT
    IVDR transition and implementation: what have we learned from the MDR?
  • 2:00 PM – 3:00 PM EDT
    Pediatric Drug Development: Failure is not an Option
  • 2:00 PM – 3:00 PM EDT
    Strategies to Leverage Patient Preference and Perspective to Support New Indications
  • 2:00 PM – 3:00 PM EDT
    Tackling a whirlwind of uncertainties:  Lessons learned on UK market access
  • 2:00 PM – 3:00 PM EDT
    Will EU IVDR implementation benefit from MDCG 2022-14 and if so, HOW?
  • 3:00 PM – 3:30 PM EDT
    Coffee & Refreshment Break
  • 3:30 PM – 4:30 PM EDT
    Live LinkedIn Feedback Session
  • 3:30 PM – 4:30 PM EDT
    Navigating the Unique Complexities of CMC Challenges for Cell Therapies
  • 3:30 PM – 4:30 PM EDT
    Non-Clinical - New
  • 3:30 PM – 4:30 PM EDT
    Overview of Select PDUFA VII Innovative Meeting Programs
  • 3:30 PM – 4:30 PM EDT
    Servicing Medical Devices – What Parts or Components SIGNIFICANTLY Change the Performance or Safety (Art 23)
  • 3:30 PM – 4:30 PM EDT
    The Art of Submission Planning: From Strategy to Filing
  • 3:30 PM – 4:30 PM EDT
    The eSTAR and I: Getting to Know the eSTAR Templates for FDA Submissions
  • 3:30 PM – 4:30 PM EDT
    The Inflation Reduction Act and Beyond: Impacts of the Evolving Reimbursement Landscape on Drug Development
  • 3:30 PM – 4:30 PM EDT
    Understand the Evolving Role of Real World Evidence
  • 4:45 PM – 5:45 PM EDT
    Companion Diagnostics: Overview of the IVDR requirements and the EMA consultation process
  • 4:45 PM – 5:45 PM EDT
    Complex Generics - New
  • 4:45 PM – 5:45 PM EDT
    Enabling Regulatory Environments to Deliver Better Access to Self Care Interventions – A Global Perspective ENABLING REGULATORY
  • 4:45 PM – 5:45 PM EDT
    Financial Acumen for Regulatory Affairs
  • 4:45 PM – 5:45 PM EDT
    International Regulator Forum
  • 4:45 PM – 5:45 PM EDT
    Predetermined Change Control Plans (PCCPS) are Now Codified in FDORA - What should you do?
  • 4:45 PM – 5:45 PM EDT
    Regulatory Collaboration Through Cloud Platforms
  • 4:45 PM – 5:45 PM EDT
    Streamlining Conformity Assessment in Medical Device Review: the FDA's ASCA Program
  • 6:30 PM – 9:30 PM EDT
    SOLD OUT - RAPS Farewell Jazz Soirée: Toasting the Future Together