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Full Schedule

Full Schedule

  • Thursday, September 9, 2021
  • 9:00 AM – 1:00 PM EST
    Pre-conference Workshop: Drug Development in EU: Regulatory Standards, Support and New Approaches
  • 1:00 PM – 8:00 PM EST
    Pre-Conference Workshop: Japan Regulatory Essentials of MDs/IVDs - Seeking Innovation Into the Regulation
  • Friday, September 10, 2021
  • 9:00 AM – 1:00 PM EST
    Pre-Conference Workshop: Drug Development in EU: Regulatory Standards, Support and New Approaches
  • 9:00 AM – 5:00 PM EST
    Pre-Conference Workshop: Global Regulatory Strategy
  • Sunday, September 12, 2021
  • 12:00 PM – 1:30 PM EST
    Opening Plenary Session: Celebrating the Profession
  • 1:30 PM – 2:00 PM EST
    Welcome Reception
  • Monday, September 13, 2021
  • 8:15 AM – 8:45 AM EST
    Wellness Experience: 30-Minute Chair Stretching
  • 9:00 AM – 9:30 AM EST
    Plenary Session: Thriving in Years of Transition
  • 9:00 AM – 4:45 PM EST
    Sponsor Solutions - Visit Sponsor Booths
  • 9:30 AM – 9:45 AM EST
    Plenary Meet the Speakers
  • 9:45 AM – 10:00 AM EST
    Visit Sponsors - Brain Break
  • 10:00 AM – 10:30 AM EST
    Companion Diagnostics (CDx) from US to Global: Current Developments and Best Practices
  • 10:00 AM – 10:30 AM EST
    Regulatory Strategy or Clinical Strategy: Where They Converge and Where They Diverge
  • 10:00 AM – 11:00 AM EST
    Artificial Intelligence in Medical Devices: Setting up the Future - Industry and Regulator Perspectives
  • 10:00 AM – 11:00 AM EST
    Cell/Gene Therapy: Emerging Technologies in Advanced Therapies
  • 10:00 AM – 11:00 AM EST
    Conversations That Matter: Interactions With Health Authorities
  • 10:00 AM – 11:00 AM EST
    Health Authority Forum: Japan
  • 10:00 AM – 11:00 AM EST
    ICH Implementation: The Transition From Convergence to Harmonization
  • 10:00 AM – 11:00 AM EST
    ISO 10993 and Biocompatibility – Test or Not to Test?!
  • 10:00 AM – 11:00 AM EST
    Leadership : Considerations for Being a Successful Remote Leader in 2021 and Beyond
  • 10:00 AM – 11:00 AM EST
    OTCs: Proprietary Name Assessment – Special Considerations for OTC Drugs
  • 10:00 AM – 11:00 AM EST
    Points for Conducting an Effective Global Clinical Trial Through Experiences in US-Japan HBD Collaborative Activities
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: Artificial Intelligence in Medical Device
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: Cell/Gene Therapy: Emerging Technologies in Advanced Therapies
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: ICH Implementation
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: ISO 10993 and Biocompatibility
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: Leadership: Considerations for Being a Remote Successful Leader in 2021 and Beyond
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: OTC's: Proprietary Name Assessment
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: Points for Conducting an Effective Global Clinical Trial Through Experiences in Us-japan HBD Collaborative Activities
  • 11:15 AM – 12:00 PM EST
    Visit Sponsors - Brain Break
  • 11:30 AM – 12:00 PM EST
    Meet the Authors: Lifecycle Management Through the Rx-to-OTC Switch
  • 12:00 PM – 12:30 PM EST
    Getting the Most out of Your Pre-Submission Meeting With FDA
  • 12:00 PM – 12:30 PM EST
    Regulatory Affairs and Merger & Acquisition – Lessons Learned Bringing Businesses Together
  • 12:00 PM – 12:30 PM EST
    Regulatory Intelligence Jam Session: Tips, Tricks and Best Practices too!
  • 12:00 PM – 1:15 PM EST
    Elevating the Role of PROs and Patient Preference Information in Regulatory Decision Making
  • 12:00 PM – 1:15 PM EST
    EU MDR/IVDR Opening Panel
  • 12:00 PM – 1:15 PM EST
    Expedited Designations and Pathways
  • 12:00 PM – 1:15 PM EST
    Health Authority Forum: CDRH
  • 12:00 PM – 1:15 PM EST
    Negotiation Skills: Mastering Career Negotiations for Success
  • 12:00 PM – 1:15 PM EST
    Pandemic Regulatory Management: COVID Challenges, Opportunities and Lessons Learned
  • 12:00 PM – 1:15 PM EST
    Preparation of Artificial Intelligence Technical Documentation and Cybersecurity Requirements for MDR and IVDR Notified Body Submissions
  • 12:00 PM – 1:15 PM EST
    Step Inside the "Real World”: Real-World Evidence Strategies in FDA Device Applications
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Elevating the Role of PROs
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: EU MDR/IVDR Opening Panel
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Expedited Designations and Pathways
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Negotiation Skills
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Pandemic Regulatory Management
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Preparation of Artificial Intelligence Technical Documentation
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Step Inside the "Real World”
  • 1:30 PM – 2:15 PM EST
    Beyond Compliance
  • 1:30 PM – 2:15 PM EST
    Building Efficiencies Into Clinical Evaluation and PMCF Strategies
  • 1:30 PM – 2:15 PM EST
    Digital Trends in Postmarket Surveillance for Medical Devices (and IVDs)
  • 1:30 PM – 2:15 PM EST
    Do you Have a Survey Methodologist on Your User Experience Team? A Case Study in User Comprehension With a Genetic Health Risk Test Report
  • 1:30 PM – 2:15 PM EST
    Lunch Break - Visit Sponsors
  • 1:30 PM – 2:15 PM EST
    Medical Writing and Submission Compilation Made Easy: Technology Solutions from Regulatory Experts
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS Germany Chapter
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS Indiana Chapter
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS Middle East and North Africa (MENA) Local Networking Group
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS New Zealand Local Networking Group
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS San Francisco Bay Area Chapter
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS Switzerland Chapter
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS United Kingdom Local Networking Group
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS Vancouver Chapter
  • 1:30 PM – 2:15 PM EST
    Panel Discussion/Q&A: Best Practices for Optimizing PMCF/PMPF and Avoiding NB Findings
  • 1:30 PM – 2:15 PM EST
    We put the "no" in Innovation: Case Studies From 20 Years of new Client Meetings
  • 1:30 PM – 2:15 PM EST
    What's Next for FDA After COVID-19?
  • 2:15 PM – 2:30 PM EST
    Meet the Speakers: Medical Writing and Submission Compilation Made Easy: Technology Solutions from Regulatory Experts
  • 2:15 PM – 2:30 PM EST
    Meet the Speakers: Best Practices for Optimizing PMCF/PMPF and Avoiding NB Findings
  • 2:15 PM – 2:30 PM EST
    Meet the Speakers: Beyond Compliance
  • 2:15 PM – 2:30 PM EST
    Meet the Speakers: Building Efficiencies into Clinical Evaluation and PMCF Strategies
  • 2:15 PM – 2:30 PM EST
    Meet the Speakers: Digital Trends in Post Market Surveillance for Medical Devices (and IVDs)
  • 2:15 PM – 2:30 PM EST
    Meet the Speakers: Do You Have a Survey Methodologist on Your User Experience Team?
  • 2:15 PM – 2:30 PM EST
    Meet the Speakers: We put the NO in Innovation: Case Studies from 20 Years of New Client Meetings
  • 2:15 PM – 2:30 PM EST
    Meet the Speakers: What's next for the FDA after COVID-19?
  • 2:30 PM – 3:00 PM EST
    Sponsor Solutions - Visit Sponsor Booths
  • 3:00 PM – 3:30 PM EST
    Change is on the Horizon for MRI Safety Labeling of Medical Devices
  • 3:00 PM – 3:30 PM EST
    Powerful Speed Networking Resulting in Meaningful Information Sharing
  • 3:00 PM – 4:00 PM EST
    Artificial Intelligence: Bias and Explainability in Algorithms
  • 3:00 PM – 4:00 PM EST
    Clinical Evaluation: Two (Somewhat) New Things That Will Be 100% Reviewed
  • 3:00 PM – 4:00 PM EST
    Decentralized Trials: Crisis Met, Future Forward
  • 3:00 PM – 4:00 PM EST
    Health Authority Forum: CBER
  • 3:00 PM – 4:00 PM EST
    The ASCA Pilot: Streamlining Conformity Assessment in Device Submissions
  • 3:00 PM – 4:00 PM EST
    The Impact of a REMS Release: A Global View
  • 3:00 PM – 4:00 PM EST
    US Drug Shortage Regulatory Requirements – FDA and Industry Perspectives
  • 3:00 PM – 4:00 PM EST
    Working at FDA
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Artificial Intelligence
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Clinical Evaluation
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Decentralized Trials
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Supply Chain - Drug Shortage
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: The ASCA Pilot
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: The Impact of a REMS Release
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Working at FDA
  • 4:15 PM – 4:45 PM EST
    Monday Wrap Up Experience
  • Tuesday, September 14, 2021
  • 8:15 AM – 8:45 AM EST
    Mindfulness LoungeTM: Waterfall Chakra Wash
  • 9:00 AM – 9:30 AM EST
    Plenary Session: Charting our Course for the Future
  • 9:00 AM – 4:45 PM EST
    Sponsor Solutions - Visit Sponsor Booths
  • 9:30 AM – 9:45 AM EST
    Plenary Session - Meet the Speakers
  • 9:45 AM – 10:00 AM EST
    Visit Sponsors - Brain Break
  • 10:00 AM – 10:30 AM EST
    Ensuring Supply Continuity Through Regulatory Strategy
  • 10:00 AM – 10:30 AM EST
    TPLC Approach for New Product Development and Sustaining Engineering: Making the Most of Postmarket Data
  • 10:00 AM – 11:00 AM EST
    Data Transparency : Begin With the End in Mind: Planning for Clinical Trial Transparency and Disclosure Requirements
  • 10:00 AM – 11:00 AM EST
    Achieving Clinical Trial Diversity – The Basics and Importance of Engaging Communities
  • 10:00 AM – 11:00 AM EST
    Career Development and Career Changes - Being a Regulatory Chief of Staff
  • 10:00 AM – 11:00 AM EST
    Drug Competition and Market Entry : Regulatory Considerations and Commercial Challenges
  • 10:00 AM – 11:00 AM EST
    Health Authority Forum: CDER
  • 10:00 AM – 11:00 AM EST
    Pre-Conference Content Included! China Regulatory 2021 Deep-dive: Major Updates, IVD Regulatory Landscape, evolving Digital Health Frameworks
  • 10:00 AM – 11:00 AM EST
    Regulatory Framework to Support Innovation: Preventing and Resolving Disputes with FDA to Support Medical Device Innovation
  • 10:00 AM – 11:00 AM EST
    UK: Challenges and Opportunities with the New United Kingdom Conformity Assessment (UKCA) Process
  • 11:00 AM – 11:15 AM EST
    Meet the Speaker Sessions
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: Achieving Clinical Trial Diversity
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: Career Development and Career Changes
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: China Regulatory 2021 Deep-dive
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: Data Transparency
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: Drug Competition and Market Entry
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: Regulatory Framework to Support Innovation
  • 11:00 AM – 11:15 AM EST
    Meet the Speakers: UK
  • 11:15 AM – 12:00 PM EST
    Impact of MDCG 2020-12 on the transition of devices containing an ancillary medicinal substance or that utilize a TSE susceptible species to MDR – Key Considerations from a NB perspective
  • 11:15 AM – 12:00 PM EST
    Meet the Authors: Fundamentals of International Regulatory Affairs, Fifth Edition, Section I: General Information, Section II: Pharmaceuticals
  • 11:15 AM – 12:00 PM EST
    Visit Sponsors - Brain Break
  • 12:00 PM – 12:15 PM EST
    Meet the Speakers: Impact of MDCG 2020-12
  • 12:00 PM – 12:30 PM EST
    Ethylene Oxide Sterilization Panel: EO Reduction Methodology and Global Regulatory Strategies and Pathways
  • 12:00 PM – 12:30 PM EST
    LATAM Regulatory & Access: Reliance and Innovation Strategic Pathways
  • 12:00 PM – 12:30 PM EST
    RAPS Volunteers Converge!
  • 12:00 PM – 1:15 PM EST
    Alternative clinical evaluation strategies: how to leverage the history of your device (WET devices) and the non-clinical data route (article 61.10)
  • 12:00 PM – 1:15 PM EST
    Building Regulatory Efficiencies Through Expedited, Reliance and Collaboration Pathways
  • 12:00 PM – 1:15 PM EST
    Drawing the Signal from the Noise in Real World Evidence for Regulatory Use
  • 12:00 PM – 1:15 PM EST
    Pediatric Drug Development: Increasing Success and Overcoming Obstacles
  • 12:00 PM – 1:15 PM EST
    Practical Post Market Surveillance
  • 12:00 PM – 1:15 PM EST
    Preparing for FDA Interactions Across the Drug Development Lifecycle: How to Positively Impact the Pathway to Approval by Engaging with the FDA Early and Often
  • 12:00 PM – 1:15 PM EST
    Risk Management and Usability: Know the Ropes and Get Safely Through the Product Life Cycle
  • 1:15 PM – 1:30 PM EST
    Meet the Speaker Sessions
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Alternative Clinical Evaluation Strategies
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Building Regulatory Efficiencies
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Drawing the Signal from the Noise in RWE for Regulatory Use
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Pediatric Drug Development
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Practical Post Market Surveillance
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers: Preparing for FDA Interactions Across the Drug Development Lifecycle
  • 1:15 PM – 1:30 PM EST
    Meet the Speakers:Risk Management and Usability
  • 1:30 PM – 2:15 PM EST
    Developing an IDMP Change Management Program
  • 1:30 PM – 2:15 PM EST
    Lunch Break - Visit Sponsors - Brain Break
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: DC Baltimore Chapter
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS Florida Chapter
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS Netherlands Chapter
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS New York New Jersey Chapter
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS Northeast Asia Local Networking Group
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS Ontario Chapter
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS Utah Chapter
  • 1:30 PM – 2:15 PM EST
    Meet and Greet: RAPS Wisconsin Chapter
  • 1:30 PM – 2:15 PM EST
    Technological Progress and Automation for MDR Implementation and Maintenance
  • 1:30 PM – 2:15 PM EST
    Transforming Regulatory Affairs Management with the Digital Thread
  • 1:30 PM – 2:15 PM EST
    Women in Regulatory: Insights to Develop Authentic Leadership
  • 2:15 PM – 2:30 PM EST
    Meet the Speakers: Developing an IDMP Change Management Program
  • 2:15 PM – 2:30 PM EST
    Meet the Speakers: Technological Progress and Automation for MDR Implementation and Maintenance
  • 2:15 PM – 2:30 PM EST
    Meet the Speakers: Transforming Regulatory Affairs Management with the Digital Thread
  • 3:00 PM – 3:30 PM EST
    Benchmarking your dossier preparation process – How does your organization compare?
  • 3:00 PM – 3:30 PM EST
    Strategy Under Uncertainty - Approaches to Increasing the Probability of Regulatory Success
  • 3:00 PM – 4:00 PM EST
    Accelerating Drug Development: The Power of Pilots & Lessons Learned from Other Drivers of Innovation
  • 3:00 PM – 4:00 PM EST
    Cell/gene Therapy: From RMAT to BLA: What are the Most Common Pitfalls Observed?
  • 3:00 PM – 4:00 PM EST
    Combination Products: Implementing Article 117 MDR Requirements Among Stake Holders
  • 3:00 PM – 4:00 PM EST
    Companion Diagnostics: EU IVDR vs FDA - Convergence and Divergence
  • 3:00 PM – 4:00 PM EST
    Health Canada Forum - Cancelled (see description)
  • 3:00 PM – 4:00 PM EST
    Performance Evaluation and Clinical Evidence
  • 3:00 PM – 4:00 PM EST
    Ready, Set, Launch! Go-to-Market Advertising and Promotion Strategies
  • 3:00 PM – 4:00 PM EST
    Regulatory Intelligence: Hiding in Plain Sight - Finding RWE Precedent in Public Information
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers Sessions
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Accelerating Drug Development
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Cell/gene Therapy - Cell/gene Therapy: From RMAT to BLA
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Combination Products
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Companion Diagnostics
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Go-to-market Advertising and Promotion Strategies
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Performance Evaluation and Clinical Evidence
  • 4:00 PM – 4:15 PM EST
    Meet the Speakers: Regulatory Intelligence
  • 4:15 PM – 4:45 PM EST
    Tuesday Wrap up Experience: Game Day!
  • Wednesday, September 15, 2021
  • 8:15 AM – 8:45 AM EST
    Wellness Experience: 30-Minute Chair Yoga
  • 9:00 AM – 9:30 AM EST
    Early Experience with Technical Documentation Assessment of Class III Orthopedic Devices Under the MDR
  • 9:00 AM – 9:30 AM EST
    FIRST LOOK: 2021 Report on The Global Regulatory Affairs Professionals Workforce
  • 9:00 AM – 9:30 AM EST
    Patient Engagement During Drug Development: Tackling the Challenges
  • 9:00 AM – 10:00 AM EST
    ArtificialUsing Intelligent Automation and Advanced Technology to Enhance Regulatory Performance
  • 9:00 AM – 10:00 AM EST
    BREXIT - Licensing Opportunities and Challenges to Overcome
  • 9:00 AM – 10:00 AM EST
    Conversations That Matter: Interactions with Health Authorities
  • 9:00 AM – 10:00 AM EST
    Fostering Cross-functional Team Success with Project Management and Alliance Management Best Practices
  • 9:00 AM – 10:00 AM EST
    Good Clinical Practice for Clinical Performance Studies in IVDs, and Performance Evaluation Process and the Performance Evaluation Report (PER)
  • 9:00 AM – 10:00 AM EST
    Navigating Europe and China UDI
  • 9:00 AM – 10:00 AM EST
    The Periodic Safety Update Report - What You Really Need to Know in 45 Minutes!
  • 9:00 AM – 10:00 AM EST
    US Policy: What has the New Biden Administration Meant for the FDA and its Regulation of Industry?
  • 9:00 AM – 1:30 PM EST
    Sponsor Solutions - Visit Sponsors
  • 10:00 AM – 10:15 AM EST
    Meet the Speakers: BREXIT
  • 10:00 AM – 10:15 AM EST
    Meet the Speakers: Good Clinical Practice for Clinical Performance Studies in Ivds
  • 10:00 AM – 10:15 AM EST
    Meet the Speakers: Navigating Europe and China UDI
  • 10:00 AM – 10:15 AM EST
    Meet the Speakers: Regulatory Strategy: Fostering Cross-functional Team Success
  • 10:00 AM – 10:15 AM EST
    Meet the Speakers: The Periodic Safety Update Report
  • 10:00 AM – 10:15 AM EST
    Meet the Speakers: US Policy
  • 10:00 AM – 10:15 AM EST
    Meet the Speakers: Using Intelligent Automation and Advanced Technology to Enhance Regulatory Performance
  • 10:15 AM – 11:00 AM EST
    Meet and Greet: RAPS Colorado Chapter
  • 10:15 AM – 11:00 AM EST
    Meet the Authors: Fundamentals of International Regulatory Affairs, Fifth Edition, Section III: Medical Devices, Section IV: Biologics, Section V: Other Product Classifications
  • 10:15 AM – 11:00 AM EST
    Visit Sponsors - Brain Break
  • 11:00 AM – 11:30 AM EST
    Improving the Recall Process; Increasing Patient Safety while Reducing Costs
  • 11:00 AM – 12:00 PM EST
    Crisis Management: Being a Regulatory Professional During a Pandemic - Professional Reflections and Lessons Learned
  • 11:00 AM – 12:00 PM EST
    How to Tackle the Biggest Challenges of SSCPs
  • 11:00 AM – 12:00 PM EST
    Lessons Learned: EU Continued Market Access – How to be Finished before 2024
  • 11:00 AM – 12:00 PM EST
    Orphan Drug / Rare Diseases
  • 11:00 AM – 12:00 PM EST
    Recent Developments in EU Regulations: Implementation of the EU MDR Requirements for Economic Operators
  • 11:00 AM – 12:00 PM EST
    Remote Inspections – Towards a New Way of Working
  • 11:00 AM – 12:00 PM EST
    The Secret Life of a NDC # - Regulatory, Safety, and Commercial Insights
  • 12:00 PM – 12:15 PM EST
    Meet the Speakers: Crisis Management
  • 12:00 PM – 12:15 PM EST
    Meet the Speakers: How to Tackle the Biggest Challenges of Sscps
  • 12:00 PM – 12:15 PM EST
    Meet the Speakers: Lessons Learned: EU Continued Market Access
  • 12:00 PM – 12:15 PM EST
    Meet the Speakers: Orphan Drug / Rare Diseases
  • 12:00 PM – 12:15 PM EST
    Meet the Speakers: Recent Developments in EU Regulations
  • 12:00 PM – 12:15 PM EST
    Meet the Speakers: Remote Inspections
  • 12:00 PM – 12:15 PM EST
    Meet the Speakers: The Secret Life of a NDC #
  • 12:15 PM – 12:45 PM EST
    Convergence 2021 Closing
  • 12:45 PM – 1:15 PM EST
    Wednesday Wrap Up Experience