- TypeWebinar
- Location San Diego, California, United States
- Date 18-01-2017
Education/Teaching/Training/Development
Finance
OTHERS
Business Development
OVERVIEW:
To satisfy QSR and ISO 13485 requirements, medical device companies must respond to field reports swiftly and compliantly.
There are certain circumstances in which a report from the field requires the device manufacturer to take steps regarding product in the field.
Product Id : 501094
Instructor : Jeff Kasoff
Why should you attend:
There are certain circumstances in which a report from the field requires the device manufacturer to take steps regarding product in the field. It is critical that the company take the required steps in the required timeframes. If not, FDA's sanctions could be so onerous as to result in the company's inability to ship product.
Areas Covered in the Session:
Who Will Benefit:
This webinar will provide valuable assistance to all regulated companies, since personnel training is a regulatory requirement in the Medical Device field. The employees who will benefit include:
IMPORTANT DATE:
Webinar Date:Â Wednesday, January 18, 2017 | 10:00 AM PST | 01:00 PM EST
Duration: 60 Minutes
For more details and updates please visit website
Netzealous LLC DBA - Compliance4All 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA.
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