Training or Development Class Information


CAPA for Medical Devices 2018


Training or Development Class Title
CAPA for Medical Devices 2018
Event Type
Training or Development Class
Training or Development Class Date
22-08-2018
Location
Fremont, California, United States

Publish / Maintain / Marketing / Hosted By
Organization Name / Organize By
Netzealous LLC DBA - Compliance4All
Organizing/Related Departments
Compliance Trainings & Seminars for all Industries
Organization Type
Organization/Company
Training or Development Class Category
Both (Technical & Non Technical)
Training or Development Class Level
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Information Technology

Accounting/Financial/Banking/Insurance

Manufacturing

Medical/Healthcare/Hospital

Location
Fremont, California, United States

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: support@compliance4All.com

Registration Fees
Available
Registration Fees Details
One Dial-in One Attendee Price: $290.00
Registration Ways
Email
Phone
Website
Address/Venue
Online  Pin/Zip Code : 94539
Official Email ID
support@compliance4All.com
Contact
Event Manager

161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA.

support@compliance4All.com

     +1-800-447-9407
   Fax No: 302-288-6884