Transitioning assays from different technologies - validation and qualification - PowerPoint PPT Presentation

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Transitioning assays from different technologies - validation and qualification

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This 1-hr virtual Webinar will help you understand the steps that must be taken when transitioning assays between different technologies – PowerPoint PPT presentation

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Title: Transitioning assays from different technologies - validation and qualification


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Transitioning assays from different technologies
- validation and qualification
www.onlinecompliancepanel.com 510-857-5896
customersupport_at_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_at_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    perform assays, to outdated technology, to new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_at_onlinecompliancepanel.com
4
Who 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
5
Reach us on
www.onlinecompliancepanel.com
Our links
www.onlinecompliancepanel.com 510-857-5896
customersupport_at_onlinecompliancepanel.com
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