Upcoming Events

Past Events
  • In-Person, Europe

    FDA Pre-Submissions: The Most Valuable Tool in Your US Regulatory Toolbox

    • 21 February 2023 - 22 February 2023
    • München, Germany
    €975 Member|€1155 Nonmember
    This 2-day workshop will review the multiple types of pre-submissions, or Q-submissions, available to manufacturers and how to leverage these to reduce the time and costs to bring medical devices to market in the U.S.
    12.0 RAC Credits
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  • In-Person, Europe

    Technical Equivalence

    • 21 February 2023 - 22 February 2023
    • München, Germany
    Price: € 975 Member | € 1,155 Nonmember
    This 2-day workshop will explore the topic of the pathway to establish technical, biological and clinical equivalence for EU conformity versus substantial equivalence pathways for the FDA.
    12.0 RAC Credits
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    REGISTER
  • In-Person, Europe

    Cybersecurity

    • 23 February 2023 - 24 February 2023
    • München, Germany
    € 975Member | € 1155Nonmember
    Don’t miss this opportunity to join your colleagues and global regulators from around the world so you can make a meaningful difference for your organization, and our industry, and most importantly, the patients.
    12.0 RAC Credits
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    REGISTER
  • In-Person, Europe

    Survivor: the FDA 510(k) Program Edition

    • 23 February 2023 - 24 February 2023
    • München, Germany
    € 975Member | € 1155Nonmember
    In this two-day, in-person workshop, you will gain an understanding of the 510(k) program and strategies to help obtain a positive clearance decision.
    12.0 RAC Credits
    LEARN MORE
    REGISTER
  • In-Person

    MDMA 2023 FDA Forum

    • 15 March 2023 - 16 March 2023
    • Palo Alto, California, USA
    Join the Medical Device Manufacturers Association (MDMA) for the annual FDA Forum. The two-day event offers insight on key regulatory issues and trends that will directly affect the regulatory and business strategies of companies of all sizes.
  • In-Person

    Risk Management for the Full Product Life Cycle: Design Concept through Post-Market Surveillance

    • 18 April 2023 - 19 April 2023
    • Rockville, Maryland, USA
    Member: $1340 | Nonmmember: $1570
    The session demonstrates an approach to sustain and use a Risk Management File throughout the product life. By attending, manufacturers will be better positioned to meet the latest regulatory requirements.
    12.0 RAC Credits
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    ADD TO CART
  • In-Person

    Software as a Medical Device

    • 18 April 2023 - 19 April 2023
    • Rockville, Maryland, USA
    Members: $1,340 | Nonmembers: $1,570
    In this two-day, in-person workshop, regulatory experts will review current and evolving regulatory requirements for software as a medical device to navigate the challenging expectations for software.
    12.0 RAC Credits
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    ADD TO CART
  • In-Person

    Cybersecurity Unauthorized (April 2023)

    • 20 April 2023 - 21 April 2023
    • Rockville, Maryland, USA
    Member: $1340 | Nonmember: $1570
    This interactive, in-person workshop will help regulatory and quality professionals develop the knowledge they need to help steer their organizations in the right direction when it comes to global cybersecurity.
    12.0 RAC Credits
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    ADD TO CART
  • In-Person

    Survivor: The FDA 510(k) Program Edition

    • 20 April 2023 - 21 April 2023
    • Rockville, Maryland, USA
    Price: Member $1340| Nonmember $1570
    2-day, in-person workshop, regulatory experts to review the current requirements & expectations of this evolving program and provide strategies to help ensure success when navigating the FDA 510(k) program
    12.0 RAC Credits
    LEARN MORE
    ADD TO CART
  • In-Person

    MedCon 2023

    • 24 April 2023 - 27 April 2023
    • Eastern Time (US & Canada)
    For 13+ years, MedCon has united the healthcare products industry to work for a better tomorrow for our patients. MedCon 2023 is hosted by the AFDO/RAPS Healthcare Products Collaborative and co-sponsored by Food and Drug Administration (FDA).
  • In-Person

    Biologics CMC: Phase Appropriate Product Development (April 2023)

    • 27 April 2023 - 28 April 2023
    • Rockville, Maryland, USA
    Member: $1340 | NonMember: $1570
    Learn how to handle technical issues affecting biologic product development challenges and expectations in the US, Europe, and other highly regulated regions.
    12.0 RAC Credits
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    ADD TO CART
  • In-Person

    Executive Development Program at the Kellogg School of Management

    • 07 May 2023 - 10 May 2023
    • Evanston, Illinois, USA
    The only leadership program dedicated to regulatory professionals like you that combines regulatory experts with faculty from one of the most prestigious business schools in the US, the Kellogg School of Management at Northwestern University.
    12.0 RAC Credits
    LEARN MORE
    ADD TO CART
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