According to the recent FDA enforcement trends, inadequate design control is frequently cited in 483s and FDA warning letters.
FDA warning letters state “Failure to establish and maintain adequate procedures to control the design of the device in order to ensure specified design requirements are met, as required by 21 CFR 820.30(a)(1).” Medical device firms are subject to design control requirements.
This webinar is intended to provide guidance on understanding, interpreting, and implementing design control procedures in a way to survive an FDA inspection. This presentation is further intended to help you establish and maintain adequate design control procedures for all classes of medical devices including IVDs. In particular, this webinar will address how to best prepare for an FDA inspection concerning design control using real case examples.
Why You Should Attend:
Understanding, interpreting, and implementing design control system requirements in a holistic manner can significantly contribute to your product quality and regulatory compliance, helping to ensure your innovative medical products to be safe and effective on a global market and saving enormous amount of your unnecessary time, efforts and investment.
In this presentation, you will get familiar with design control requirements and the FDA inspection concerning design control systems applicable to all types of medical devices including IVDs. This webinar is a must for medical device and IVD firms including anyone interested in the topics from other industry.
- Statutes and Regulations Governing Medical Devices
- Introduction and Definitions
- Design and Development Planning
- Design Input and Design Output
- Design Review
- Design Verification And Validation
- Design Transfer and Design Changes
- Design History File (DHF), Device History Record (DHR) and Device Master Record (DMR)
- FDA Inspection for Design Control
- Common Mistakes and How to Avoid
- How to Prepare for FDA inspection for Design Control
- Design Control: Best Practices
- Speaker’s Recommendation and Suggestions on PASS-IT Solutions
- R&D Departments
- Quality Departments
- Compliance Departments
- Regulatory Affairs Departments
- Clinical Affairs Professionals
- Anyone Interested in the topic