RAPS is closely monitoring developments in the Coronavirus (COVID-19) outbreak. See our public safety page for the latest updates.

RAPS is closely monitoring developments in the Coronavirus (COVID-19) outbreak. See our public safety page for the latest updates.

Upcoming Events

Past Events
  • Online Workshop

    SOLD OUT – EU In Vitro Diagnostics Regulations (IVDR)

    • 09 June 2020 - 10 June 2020
    The transition to meeting the new IVDR requirements involves significant preparation and data generation to be ready for additional notified body review and scrutiny. Join RAPS for this workshop and prepare to comply fully with the new regulations.
    12.0 RAC Credits
    REGISTER
  • Online Workshop

    RAPS/TOPRA Inter-regulatory and Stakeholder Workshop: Alignment of Global ‘Combination’ Products Regulations

    • 10 June 2020 - 11 June 2020
    Join RAPS, TOPRA and regulatory leaders for a workshop that will provide an opportunity to learn about the different global approaches to 'combination' product regulation.
    8.0 RAC Credits
    REGISTER
  • Online Workshop

    China NMPA Regulations and Processes for Medical Devices

    • 17 June 2020 - 18 June 2020
    Regulatory professionals need to have sufficient understanding of China’s NMPA regulations, processes and skills to navigate the NMPA system. This workshop is structured to provide attendees with the fundamental knowledge about the NMPA regulations,
    12.0 RAC Credits
    REGISTER
  • Online Workshop

    Root Cause Investigation for CAPA

    • 23 June 2020 - 24 June 2020
    Investigative tools used to identify technical root causes, systemic root causes, corrective and preventive actions, as well as control plans to monitor and prevent recurrence.
    12.0 RAC Credits
    REGISTER
  • Online Workshop

    Introduction to Electronic Regulatory Submissions in the eCTD Format - July 2020

    • 14 July 2020 - 15 July 2020
    Organizations need to understand both the underlying CTD structure and their options for implementing operational changes that will lead to successful electronic applications. Join RAPS for a two-day workshop on regulatory submissions in eCTD format.
    8.0 RAC Credits
    REGISTER
  • Online Workshop

    Intermediate Course for Regulatory Submissions in eCTD Format - July 2020

    • 16 July 2020 - 17 July 2020
    If you have a working knowledge of the CTD structure and need to learn how to correctly apply it to electronic submissions, or if you need to know what is required to comply with the FDA’s May 2020 guidances, this two-day workshop is for you.
    10.0 RAC Credits
    REGISTER
  • Online Workshop

    Software as a Medical Device

    • 28 July 2020 - 29 July 2020
    This workshop will be particularly beneficial to regulatory professionals, QA professionals and application developers who are responsible for managing and planning regulatory compliance for software products.
    12.0 RAC Credits
    REGISTER
  • Online Workshop

    Biologics CMC Workshop: Current Trends, Future Trends and Regulatory Challenges - September 2020

    • 29 September 2020 - 30 September 2020
    This workshop provides an overview of chemistry, manufacturing and control (CMC) regulatory requirements and best practices associated with biologic and biosimilar products, with emphasis on requirements in the US, Europe and other regulated regions.
    12.0 RAC Credits
    REGISTER
  • Online Workshop

    Introduction to Electronic Regulatory Submissions in the eCTD Format - October 2020

    • 20 October 2020 - 21 October 2020
    Organizations need to understand both the underlying CTD structure and their options for implementing operational changes that will lead to successful electronic applications. Join RAPS for a two-day workshop on regulatory submissions in eCTD format.
    8.0 RAC Credits
    REGISTER
  • Online Workshop

    Intermediate Course for Regulatory Submissions in eCTD Format - October 2020

    • 22 October 2020 - 23 October 2020
    If you have a working knowledge of the CTD structure and need to learn how to correctly apply it to electronic submissions, or if you need to know what is required to comply with the FDA’s May 2020 guidances, this course is for you.
    10.0 RAC Credits
    REGISTER