Upcoming Events

Past Events
  • Virtual Programs

    Cybersecurity Unauthorized (Feb 2023)

    • 07 February 2023 - 08 February 2023
    • Eastern Time (US & Canada)
    Members: $970 | Nonmembers: $1,150
    This 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 expectations.
    12.0 RAC Credits
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    ADD TO CART
  • Virtual Programs

    Business Writing for Regulatory Professionals: Making It Easy (Feb 2023)

    • 15 February 2023
    • Eastern Time (US & Canada)
    Member: $230 | NonMember: $270
    Learn to write documents in a clear and well‐organized manner under short deadlines, that are correct, complete and concise.
    2.0 RAC Credits
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  • Virtual Programs

    How to Submit a DMF to China’s NMPA: Practice Points and Latest Updates

    • 16 February 2023
    • Eastern Time (US & Canada)
    Member: $175 | NonMember: $200
    This workshop will provide a thorough understanding of China NMPA Drug Master Filings (DMF). By attending, regulatory professionals and manufacturers will better position themselves to meet new requirements.
    1.5 RAC Credits
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  • Virtual Programs

    RAPS Webcast: Streamlining Conformity Assessment in Device Submissions: FDA’s ASCA Program

    • 16 February 2023
    • Eastern Time (US & Canada)
    Price: Free
    Introductory webcast for participants to the webcast for participants to the FDA's ASCA, a program in which manufacture.rs may contract with ASCA-accredited test labs to perform testing to certain consensus standards
    1.0 RAC Credits
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  • 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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    REGISTER
  • 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
  • Virtual Programs, Chapter Events

    DC/ Baltimore Chapter: FDA Compliant Use of Smartphones, Apps and Technology in Clinical Trials

    • 22 February 2023
    • Eastern Time (US & Canada)
    Member: $0| Nonmember: $25
    Use of wearable devices and smart technology is increasing in clinical trials. This program will discuss the use of Smartphones, Apps and other technology in terms of FDA compliance and practical concerns
    1.0 RAC Credits
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  • 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
  • Virtual Programs

    RAPS Webcast: MDR by The Numbers

    • 23 February 2023
    • Mountain Time (US & Canada)
    Free
    MDR implementation cold, hard, numbers: results of research on recent MDCG guidance, industry and Notified Body surveys, and interviews with stakeholders (including NB) on experiences with implementation.
    1.5 RAC Credits
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  • 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
  • Virtual Programs

    Sponsored Webcast: Insights and Actions from the 2023 Medtech Regulatory Performance Report

    • 23 February 2023
    • Eastern Time (US & Canada)
    Price: Free
    The 2022 Medtech Regulatory Performance survey of 200 medtech regulatory professionals yielded some expected and some unexpected results. We will explore the findings and regulatory predictions for 2023.
    1.0 RAC Credits
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  • Virtual Programs, Chapter Events

    San Francisco Bay Area Chapter: Wellness Device or Medical Device?

    • 24 February 2023
    • Pacific Time (US & Canada)
    Members: Free | Nonmembers: $25
    Learn the difference between medical and wellness devices, the importance of manufacturer claims, and how those claims can affect the classification of devices.
    1.0 RAC Credits
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    ADD TO CART
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