Transitioning Assays from Different Technologies - Validation and Qualification

Duration: 60 Minutes
This 1-hr webinar will help you understand the steps that must 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 and develop a transition plan to make sure results could be easily compared between the two technologies.
Transitioning Assays From Technologies
Instructor: Todd Graham
Product ID: 500578

Why Should you Attend:
Laboratories need transition of technologies all 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 From new ways to perform assays, to outdated technology, to new equipment pushes to the various needs of end users, assays need to switch between technologies on a regular basis.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 must be able to easily and robustly transition assays from one technology to another. With this webinar, you will be able to fully understand how your assay is currently running and make a 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, 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 also get trained to develop a validation plan that will allow you to embrace the new technology fearlessly.

Objectives of the Presentation:
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:
  • Senior management
  • Quality Assurance
  • Research and Development
$375
Recorded Session for one participant
Get life time access with download option!
Book This Course
  $500.00 Training CD
Free shipment within 7 Working Days, from the date of webinar completion. Get life time access for unlimited participants.
  $600.00 Flash Drive
Free shipment within 7 Working Days, from the date of webinar completion. Get life time access for unlimited participants.
For multiple location please contact our customer care team +1-510-857-5896.
Do you want to Host
this webinar at your Organization!
Call us at +1-510-857-5896
Email us at webinar@onlinecompliancepanel.com
Minimum 10 attendees
How it works
Live Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • The webinar joining link, username and password for joining the webinar will be updated on your OCP Account 24 hours prior to the webinar
  • Presentation handouts in Downloadable PDF format will be updated on your OCP Account 24 hours prior to the live session
  • Login to the audio conference on the scheduled date and time
  • Get answers to your queries through interactive Q&A sessions via chat at the end of the session
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Todd Graham is a masters-level bench scientist and medical technologist with a host of experience in both clinical diagnostics and biotechnology fields. He has worked for a number of start-up firms in the clinical diagnostics and biotechnology industries, as well as worked for larger firms within both industries. He has a broad level of expertise in assay development for quality control, pharmaceutical development and clinical diagnostics. His particular levels of expertise are in molecular diagnostics, PCR, ELISA, quality control and training of bench level personnel in clinical diagnostics and biotechnology. He has established a consultancy to assists academic labs in transitioning their research to industry by verifying and improving the quality of their work.


View More