The webinar will speak about the Transitioning Assays from different Technologies

1. Transitioning assays from different technologies -
validation and qualification
www.onlinecompliancepanel.com | 510-857-5896 | customersupport@onlinecompliancepanel.com

2. 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.
www.onlinecompliancepanel.com | 510-857-5896 | customersupport@onlinecompliancepanel.com

3. 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perform assays, to outdated technology, to new equipment pushes to the various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. 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.
www.onlinecompliancepanel.com | 510-857-5896 | customersupport@onlinecompliancepanel.com

4. Who can Benefit:
Senior management
Quality Assurance
Research and Development
Live Session - How it works
• Username and Password will be sent
to you 24 hours prior to the webinar
• Presentation handouts in pdf formate
will be mailed to you
• Login to the session using the
username and password provided to
you
• Get answer to your queries through
interactive Q&A sessions via chat
• Please let us know your thoughts and
views at the end of webinar, your
valuable feedback will help us
improve
• Get certification of attendance.
Recorded Session - How it works
• A link will be provided to you upon
purchase of the recorded session
• Please click on the link to access the
session
• Presentation handouts in pdf formate
will be mailed to you
• Get certification of attendance.
www.onlinecompliancepanel.com | 510-857-5896 | customersupport@onlinecompliancepanel.com

5. Reach us on :
www.onlinecompliancepanel.com
Our
links
www.onlinecompliancepanel.com | 510-857-5896 | customersupport@onlinecompliancepanel.com