The RAPS store will be under maintenance Saturday, 17 April between 5 AM and 12 PM EST. Store functionality may be unavailable at times during this window.
We apologize for any inconvenience caused during this time.

Upcoming Events

Past Events
  • Online Workshop

    SOLD OUT - Biologics CMC: Future Trends, Current Trends and Regulatory Challenges

    • 13 April 2021 - 14 April 2021
    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
    LEARN MORE

    ADD TO CART
  • Online Workshop

    SOLD OUT – Software as a Medical Device- April 2021

    • 14 April 2021 - 15 April 2021
    Our April workshop is sold out, but join us in July for a review of the current and evolving global regulatory requirements affecting software as a medical device (SaMD): raps.org/Events/software-as-a-medical-device--july-2021.
    12.0 RAC Credits
    LEARN MORE

    ADD TO CART
  • Online Workshop

    Talking to Decision Makers: What to Say and How to Say It

    • 23 April 2021
    Position yourself for future success by learning how to succinctly communicate with executives. This event will teach you how to explain issues clearly and how to make yourself an invaluable asset to senior leadership within your organization.
    1.5 RAC Credits
    LEARN MORE

    ADD TO CART
  • Online Workshop

    US Regulatory Essentials, Devices

    • 05 May 2021 - 06 May 2021
    This online workshop offers a comprehensive overview of U.S. regulatory affairs for medical devices and IVDs. It will cover laws, regulations, FDA guidance, strategies for FDA submissions, advertising and labeling, post-market compliance, and more.
    12.0 RAC Credits
    LEARN MORE

    ADD TO CART
  • Online Workshop

    Expedited Pathways (US/Global) – Medical Device

    • 08 June 2021 - 09 June 2021
    Led by a veteran regulatory manager, this workshop will focus on expedited pathways by FDA, EU, China NMPA and other regulatory agencies from major global markets as to map out a pathway to bring products to market as fast as possible.
    12.0 RAC Credits
    LEARN MORE

    ADD TO CART
  • Online Workshop

    US Regulatory Essentials, Pharmaceuticals

    • 09 June 2021
    An overview of laws, regulations and guidance affecting US regulation of biologics and pharmaceutical products, this workshop is tailored for new to intermediate level professionals and those preparing for the RAC Drugs examination.
    6.0 RAC Credits
    LEARN MORE

    ADD TO CART
  • Online Workshop

    IVDR: Implementation NOW - Learn from early adaptors

    • 16 June 2021 - 17 June 2021
    Designed to build practical experience and current thinking, this workshop will look at what we know and have learned in the last year, building the new requirements and processes into the QMS to support pre- and post-market devices.
    12.0 RAC Credits
    LEARN MORE

    ADD TO CART
  • Online Workshop

    Biologics CMC: Phase Appropriate Product Development

    • 13 July 2021 - 14 July 2021
    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
    LEARN MORE

    ADD TO CART
  • Online Workshop

    Software as a Medical Device- July 2021

    • 27 July 2021 - 28 July 2021
    Join us for a review of the current and evolving global regulatory requirements affecting software as a medical device (SaMD).
    12.0 RAC Credits
    LEARN MORE

    ADD TO CART
  • Online Workshop

    China NMPA Workshop 2021 – In Vitro Diagnostics (IVD)

    • 16 August 2021 - 17 August 2021
    Led by veteran regulatory managers, this workshop will present a systematic review of all elements in the Chinese regulations from clinical trial to quality management, product registration and post market surveillance.
    12.0 RAC Credits
    LEARN MORE

    ADD TO CART
  • Online Workshop

    Cybersecurity Unauthorized

    • 05 October 2021 - 06 October 2021
    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
    LEARN MORE

    ADD TO CART
  • Online Workshop

    Introduction to Regulatory Submissions in the eCTD Format - October 2021

    • 11 October 2021 - 12 October 2021
    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.
    12.0 RAC Credits
    LEARN MORE

    ADD TO CART
RAPS EventsRSS 2.0