Statistical Rationale 2016 - Conference about Sample Size and Statistical Rationale for Medical Device Packaging Validations
Date2016-01-18
Deadline2016-01-17
VenueOnline Event, USA - United States
KeywordsPackage validation testing; Process Validation; Medical Devices Training
Websitehttps://bit.ly/1Xo2XVW
Topics/Call fo Papers
Overview:
Compliance to ISO 11607, Parts 1 and 2 require that Packaging Validations include the development of a statistical rationale to support the testing conclusions of sterile barrier systems and packaging processes. Learn the basics of a process for developing a validation statistical rationale for packaging sterile barrier systems and processes.
Areas Covered in the Session:
Statistical Rationales-the importance and application of developing an appropriate sample size for testing
Compliance and guidance for:
Medical device sterile barrier systems
Determining sample size for sterile barrier systems (packaging systems)
A process for developing an appropriate and statistically valid test population
Summary of key takeaways of non-statistically significant survey of medical device companies on statistical rationales
Wrap Up
Question and answer
Who Will Benefit:
Packaging and Quality Engineers
Packaging and Quality Managers
Test Engineers
Speaker Profile:
Karen K. Greene is currently Vice President, Life Packaging Technology LLC, a packaging engineering consulting and services firm. She has been a packaging engineering industry professional for over 30 years. Ms. Greene holds a Bachelor of Arts, Biology, degree from Holy Cross College in Worcester, MA and a professional certificate in engineering management from University of CA, San Diego. She is a certified packaging professional, CPP, the Co- President of the southern California Chapter of the Institute of Packaging Professionals and is a committee chairperson of the IoPP Medical Device Packaging Technical Committee. Ms. Greene is a member of the ASTM F02, Flexible Barrier Packaging committee. She is an ISTA 7E (thermal design and validation) certified auditor.
Contact Detail:
NetZealous - Compliance4All,
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539, USA.
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com
http://www.compliance4all.com/
Event Link : http://bit.ly/1Xo2XVW
Compliance to ISO 11607, Parts 1 and 2 require that Packaging Validations include the development of a statistical rationale to support the testing conclusions of sterile barrier systems and packaging processes. Learn the basics of a process for developing a validation statistical rationale for packaging sterile barrier systems and processes.
Areas Covered in the Session:
Statistical Rationales-the importance and application of developing an appropriate sample size for testing
Compliance and guidance for:
Medical device sterile barrier systems
Determining sample size for sterile barrier systems (packaging systems)
A process for developing an appropriate and statistically valid test population
Summary of key takeaways of non-statistically significant survey of medical device companies on statistical rationales
Wrap Up
Question and answer
Who Will Benefit:
Packaging and Quality Engineers
Packaging and Quality Managers
Test Engineers
Speaker Profile:
Karen K. Greene is currently Vice President, Life Packaging Technology LLC, a packaging engineering consulting and services firm. She has been a packaging engineering industry professional for over 30 years. Ms. Greene holds a Bachelor of Arts, Biology, degree from Holy Cross College in Worcester, MA and a professional certificate in engineering management from University of CA, San Diego. She is a certified packaging professional, CPP, the Co- President of the southern California Chapter of the Institute of Packaging Professionals and is a committee chairperson of the IoPP Medical Device Packaging Technical Committee. Ms. Greene is a member of the ASTM F02, Flexible Barrier Packaging committee. She is an ISTA 7E (thermal design and validation) certified auditor.
Contact Detail:
NetZealous - Compliance4All,
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539, USA.
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com
http://www.compliance4all.com/
Event Link : http://bit.ly/1Xo2XVW
Other CFPs
- Conference about Sterile Medical Packaging Design - 7 Essentials
- Conference about Does Anyone Care About SOX Anymore?
- Conference about SOPs for Clinical Trials - Regulatory Requirement and Key to Effective Management
- Conference about EHS Leading Indicators - Facing Front While Looking Back
- Conference about Faster Payments: Evolution or Revolution?
Last modified: 2015-11-27 17:54:11