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Event Details


Validation Sampling Plans for Process Validation [Latest]

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Who should attend?

Compliance Officer QA/QC Engineers and Management Process Engineers and Management Design Engineer and Management Regulatory and CAPA Personnel Statisticians


Select from among these sampling plans that plan which offers the best
balance between the number of units tested and the risk of failing the
How to identify when sampling plans for other properties are required for
things like precision, accuracy, homogeneity and failure rates

Why should you Attend:
In the medical device industry acceptance sampling plans are required for
Validation/Verification/Effectiveness studies that must:
Be based on a written procedure
Aligns the plans to risk
Provides a valid statistical rationale

Areas Covered in the Session:
Claims that can be made when passing a sampling plan
How to select a sampling plan to make a specific claim
Different types of sampling plans including single, double and variables
How to reduce the number of units tested

Who Will Benefit:
Process Engineers and Management
Design Engineer and Management
Regulatory and CAPA Personnel

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


One Dial-in One Attendee Price: $150.00


Event Manager

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