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 CAPA
Lessons Learned from 483s and warning letters
CAPA Process
Common problems CAPA
How to structure your CAPA process for effectiveness and
efficiency
How to use IT tools to monitor and maintain your CAPAs

Who Will Benefit:
Quality Systems Specialists
Document Control Specialists
Quality and Compliance Specialists
Internal Auditors and Managers
Training 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: +1-800-447-9407
Email: [email protected]

http://www.compliance4all.com/control/w_product/~product_id=502034LIVE?channel=speedycourse_Aug_2018_SEO

One Dial-in One Attendee

Price: $290.00