Is Your Medical Device Software 510k Ready? is a webinar that covers topics such as:
- Pertinent and required Guidances that the FDA Recognizes in support of submitting a 510(k) for software
- What is required to have in place for Quality Systems to ensure your Software submission will be accepted for approval by the FDA for review to prevent costly time to market delays
- Exactly what software documentation needs to be prepared and how for a Class II/B/Moderate Level of Concern for the Software Portion to ensure
- How to ensure the software documentation is prepared correctly specifically for the software portion of the submittal so that it will be in compliance preventing delays of the 510(k) approval
- Potential audit risks and serious findings post submittal that can block their ability to ultimately sell their product successfully
- What is expected to have in place for compliance for your company during the preparation of a 510(k) to prevent this risk
- A faster 510(k) approval because the documentation is complete and comprehensive
- Costly time to market issues because 510(k) has been rejected completely because of software
Is Your Medical Device Software 510k Ready? is intended for:
- Medical Device Software Quality Assurance Engineers
- Medical Device Software Regulatory professionals
- Medical Device Software Company Senior Management
- Medical Device Software Quality Senior Management
- Medical Device Quality Senior Management
- Medical Device Quality Engineers
