Medical Device 2012 - Understanding Design Controls for Medical Devices
Date2012-02-23
Deadline2012-02-23
VenuePalo Alto, USA - United States
KeywordsDesign Control; Medical Device Design Control; Design Control Requirements; Documentation Requirements; Design Control Process; Design Documentation; Device Design Review
Topics/Call fo Papers
This webinar will cover the basics of design controls for medical devices, and provide recommendations for implementation of a compliant design control system. Also discussed will be design control requirements for devices already in distribution. Documentation requirements for each design stage will be included as well.
Why You Should Attend:
Prior to introduction of a new device, or even a modified design for an existing device, a systematic process must be followed. This process must ensure that all requirements are met. A firm's design control process must meet all regulatory requirements, but at the same time not be as unwieldy as the present a barrier to timely market introduction. This webinar will cover the basics of design controls, and provide recommendations for implementation of a compliant design control system. Also discussed will be design control requirements for devices already in distribution. Documentation requirements for each design stage will be included as well.
Other CFPs
- Advanced Methods of Root Causes Analysis for ISO 14971 Risk Reduction
- Complaint Handling in Compliance with FDA and ISO Regulations
- Medical Device Regulations and Law in the US, EU and Canada
- Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment
- Software Verification and Validation Planning and Implementation
Last modified: 2012-01-23 15:20:31