Thank you for attending the 16th Annual FMMC Symposium in St. Petersburg, Florida. We hope you found this year’s conference to be informative, and hopefully, you gained new valuable insights from the “FDA Priorities & Compliance ‘Hot Topics'” and “FDA Transition: Update on Proposed Rule Aligning QSR with ISO 13485” super sessions we moderated with our FDA colleagues.
Furthermore, if you were able to attend our special workshop session, “Practical Application of Risk Management for Medical Devices (ISO 14971:2019)”, we appreciate your attendance and hope you took away some practical ways to apply and implement your risk management program. As a thank you, we are providing a copy of the presentation and some of the associated templates/handouts we presented. Please complete the form to access these materials.
If you have any questions or need additional information regarding the FDA Super Session or our Risk Management training, please feel free to contact us using the form. We also welcome any requests for our consulting, auditing, and training services and are happy to schedule a call.
