Medical Device Submissions Workshops

Feb 05, 2024—Feb 09, 2024


510(k) and De Novo Submissions Workshop: February 5-6, 2024
IDE Submissions Workshop: February 7, 2024
PMA Submissions Workshop: February 8-9, 2024

Join us in February for our three back-to-back, Medical Device Submissions Workshops, including: 510(k) and De Novo; Investigational Device Exemption (IDE); Premarket Approval (PMA)! After years of hosting this event virtually, we’re excited to offer a hybrid experience that includes a virtual and in-person option in our Washington, D.C. office! The hybrid format allows us to offer a more comprehensive and interactive experience, while providing the same access to real-world case studies, tips and best practices directly from the FDA and leading industry experts. These workshops are instrumental in guiding professionals through the intricate world of medical device submissions, so if you’re new to medical device regulatory affairs, or looking to strengthen your foundational knowledge, this is the perfect program for you. Sign-up below to be the first to receive more information on these can’t-miss workshops!

Who should attend?

  • Medical device professionals new to the FDA regulatory submission process
  • Regulatory Affairs Professionals
  • Regulatory Compliance Professionals
  • Quality Assurance Professionals
  • Regulatory Affairs Rotational Associates