Compliance4All has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements. Compliance4All offers path breaking professional training solutions to organizations that help them address pain areas and overcome the challenges and difficulties associated with meeting regulatory requirements.

A broad variety of organizations that work in various industries and activities that require regulatory compliance trainings benefits in major ways from Compliance4All’s professional trainings. These trainings are relevant, focused and cost effective, and are on matters that relate to the day-to-day work that regulatory professionals carry out. 

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Test Method Validation to Verify the Performance of a Medical Device

Start Date : April 4, 2019
End Date : April 4, 2019
Time : 10:00 am to11:30 am

Phone : 8004479407
Email : compliance4all14@gmail.com

Description

Overview:


Those who work with process optimization and validation focus on optimizing a process and reducing variability. Those working on Test Method Validation, on the other hand, focus on discerning between process variation and measurement error from the test method itself.


 


Why should you Attend:


This webinar will help you better understand Test Method Validations to verify the performance of a Medical Device, global reference standards, the FDA requirements and how to perform successful TMV to ensure your inspection of verification is effective, using detailed real-life case studies.


 


Areas Covered in the Session:


When should Methods be Validated?


Qualification vs Validation


Types of Test Method Validations


How to perform successful test method validations


 


Who Will Benefit:


Manufacturing Engineers


Regulatory Affairs Teams


Quality Assurance & Quality Control Teams


Operations Teams


Document Control


 


Speaker Profile:


Jose Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device industry specializing in manufacturing, process development, tooling, and quality systems. Prior to working full time as a consulting partner for Atzari Consulting, Jose served as Director of Manufacturing Engineering at Boston Scientific and as Quality Systems Manager at Stryker Orthopedics, where he introduced process performance, problem solving, and quality system methodologies.


 


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


 


Contact Detail:


Compliance4All DBA NetZealous,


Phone: +1-800-447-9407


Email: compliance4all14@gmail.com

Organized by

Organized by compliance4all14

Netzealous LLC DBA - Compliance4All ,
161 Mission Falls Lane, Suite 216,

Compliance4All has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements. Compliance4All offers path breaking professional training solutions to organizations that help them address pain areas and overcome the challenges and difficulties associated with meeting regulatory requirements.

A broad variety of organizations that work in various industries and activities that require regulatory compliance trainings benefits in major ways from Compliance4All’s professional trainings. These trainings are relevant, focused and cost effective, and are on matters that relate to the day-to-day work that regulatory professionals carry out. 

Tel: 8004479407
Mobile: 8004479407
Email: compliance4all14@gmail.com
Website: http://www.compliance4all.com/


Event Categories: Health & Nutrition.




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