2014 - Transitioning assays from different technologies: validation and qualification
Date2014-05-30
Deadline2014-05-30
VenueVirtual Webinar, USA - United States
KeywordsValidation and qualification; New assay technology; Assay transfer plan
Topics/Call fo Papers
Instructor: Todd Graham
Description:
This 1-hr virtual seminar will help you understand the steps that need to be taken when transitioning assays between different technologies. It will make sure you have a full understanding of the legacy technology and the current technology, develop a transition plan and make sure that results can be easily compared between the two technologies.
Why Should you Attend:
Laboratories need to transition technologies all of the time. From new ways to perform assays, to outdated technology, to new equipment pushes to the various needs of end users, assays need to switch between technologies on a regular basis. One needs to be able to easily and robustly transition assays from one technology to another. With this seminar, you will be able to fully understand how your assay is currently running and make note of what the new technology should be able to do. Then you will learn how to slowly get the new technology up and running, validating the quality system, equipment and the assay itself. You will learn what you need to understand in the process of transitioning old samples onto the new system and deal with any potential issues. Finally, you will develop a final validation plan that will allow you to embrace the new technology fearlessly.
Objectives of the Presentation:
This webinar will help you identify the key steps needed to take in order to transition assays between different technologies. This will allow you to shift assays from one technology to another as demanded by laboratory needs. The webinar will include the following critical information you will need:
Understanding your current assay
Validating your new assay technology
Creating an assay transfer plan
Implementing and performing an assay transfer plan
Monitoring the results of assay transfer validation
Green-lighting the new technology
Who can Benefit:
This topic applies to personnel / companies in the medical diagnostic industry. The employees who will benefit most include:
Senior management
Quality Assurance
Research and Development
Register Now:
http://www.onlinecompliancepanel.com/ecommerce/web...
Online Compliance Panel LLC
38868 Salmon Ter
Fremont, CA, USA
94536
Toll Free: 1-510-857-5896
Description:
This 1-hr virtual seminar will help you understand the steps that need to be taken when transitioning assays between different technologies. It will make sure you have a full understanding of the legacy technology and the current technology, develop a transition plan and make sure that results can be easily compared between the two technologies.
Why Should you Attend:
Laboratories need to transition technologies all of the time. From new ways to perform assays, to outdated technology, to new equipment pushes to the various needs of end users, assays need to switch between technologies on a regular basis. One needs to be able to easily and robustly transition assays from one technology to another. With this seminar, you will be able to fully understand how your assay is currently running and make note of what the new technology should be able to do. Then you will learn how to slowly get the new technology up and running, validating the quality system, equipment and the assay itself. You will learn what you need to understand in the process of transitioning old samples onto the new system and deal with any potential issues. Finally, you will develop a final validation plan that will allow you to embrace the new technology fearlessly.
Objectives of the Presentation:
This webinar will help you identify the key steps needed to take in order to transition assays between different technologies. This will allow you to shift assays from one technology to another as demanded by laboratory needs. The webinar will include the following critical information you will need:
Understanding your current assay
Validating your new assay technology
Creating an assay transfer plan
Implementing and performing an assay transfer plan
Monitoring the results of assay transfer validation
Green-lighting the new technology
Who can Benefit:
This topic applies to personnel / companies in the medical diagnostic industry. The employees who will benefit most include:
Senior management
Quality Assurance
Research and Development
Register Now:
http://www.onlinecompliancepanel.com/ecommerce/web...
Online Compliance Panel LLC
38868 Salmon Ter
Fremont, CA, USA
94536
Toll Free: 1-510-857-5896
Other CFPs
Last modified: 2014-05-27 22:12:30