Title: Transitioning assays from different technologies - validation and qualification
1Transitioning assays from different technologies
- validation and qualification
www.onlinecompliancepanel.com 510-857-5896
customersupport_at_onlinecompliancepanel.com
2Instructor 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_at_onlinecompliancepanel.com
3Why 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perform assays, to outdated technology, to new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_at_onlinecompliancepanel.com
4Who can BenefitSenior managementQuality
AssuranceResearch 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
QA 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_at_onlinecompliancepanel.com
5Reach us on
www.onlinecompliancepanel.com
Our links
www.onlinecompliancepanel.com 510-857-5896
customersupport_at_onlinecompliancepanel.com