Medical Device Employee Training - 2017

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Category Medical Device, FDA Webinar, Cgmp Training, medical device companies, medical device manufacturers, medical companies, top medical device companies, medical instruments, Quality Associates

Deadline: May 16, 2017 | Date: May 17, 2017

Venue/Country: Online, U.S.A

Updated: 2017-03-21 16:25:09 (GMT+9)

Call For Papers - CFP

This is especially true for start-up and other small medical device companies, or rapidly growing companies. Specific FDA training requirements will be presented.

Why should you Attend:

This presentation will provide information and tips on best practices for assuring your employees are properly trained and you can demonstrate it. Improperly or inadequately trained employees lead to both product and process nonconformities.

Areas Covered in the Session:

Review of types of training requirements from the FDA and ISO 13485

Providing examples of ways to document training needs for employees

Looking at various ways to monitor the effectiveness of each type of training

Who Will Benefit:

Quality Management

Human resource managers

Quality Specialists

Production Supervisors

Speaker Profile:

Betty Lane has over 30 years' experience in Medical Device quality assurance and regulatory affairs. She is the founder and President of Be Quality Associates, LLC, a consulting company helping small and medium sized medical device and diagnostic companies implement and improve their quality systems.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: supportcompliance4All.com