Medical Devices - Complying With 820.250 Statistical Methods

Website https://www.compliance4all.com/control/w_product/~product_id=502291LIVE?channel=coursefordoctors_Feb | Edit Freely

Category Statistical Methods, Sampling Plans, Internal Auditors, types of sampling plans, regulatory risk, credit risk management process, compliance trainings, statistical procedures, statistical regulations

Deadline: February 03, 2019 | Date: February 04, 2019

Venue/Country: Online, U.S.A

Updated: 2018-12-07 14:53:55 (GMT+9)

Call For Papers - CFP

In this webinar you will learn how to structure your statistical procedures to ensure compliance, and how to avoid these and how to fully comply with the statistical regulations.

Why should you Attend:

Two of common 483 and Warning letter items are:

Lack of valid statistical rationale

Inadequate trending of Quality data

Learn how to avoid these and how to fully comply with the statistical regulations

Areas Covered in the Session:

Important elements for each procedure

Valid statistical rational

Structuring the procedures to reduce the training burden

Deviating from procedures

Handling when there is not a procedure

Who Will Benefit:

Corporate and Division Management

Regulatory Management and Personnel

Internal Auditors

QA/QC Engineers and Management

Process Engineers and Management

Design Engineer and Management

Statisticians

Speaker Profile:

Wayne Taylor is a leading expert on the application of Statistics to the Medical Device and other FDA regulated industries. His new book Statistical Procedure for the Medical Device Industry sets the standard for applying statistics in compliance with Section §820.250, Statistical Techniques of the Code of Federal Regulations.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: compliance4all14gmail.com