CAPA for Medical Devices 2018

Overview: You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. In this 3-hour webinar, you'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you.
Why should you Attend:CAPA is the cornerstone of an effective Quality Management System. Yet, it frequently perceived as a burdensome and bureaucratic exercise. Many companies struggle to establish and maintain a CAPA program that is efficient and effective. An ineffective CAPA System leads to disastrous consequences such as medical device reports, recalls, 483s, and warning letters.
Areas Covered in the Session:FDA and NB expectations for CAPALessons Learned from 483s and warning lettersCAPA ProcessCommon problems CAPAHow to structure your CAPA process for effectiveness and efficiencyHow to use IT tools to monitor and maintain your CAPAs
Who Will Benefit:Quality Systems SpecialistsDocument Control SpecialistsQuality and Compliance SpecialistsInternal Auditors and ManagersTraining Specialists
Speaker Profile:Susanne Manz MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities.
Event Fee: One Dial-in One Attendee Price: US $290.00
Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: support@compliance4All.com