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How To Switch Assay Platforms without Sacrificing Quality?

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Course Description:

This Webinar 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 From new ways to perform assays, to outdated technology, to new equipment pushes to the various needs of end users, assays need to switch between technologies on a regular basis.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.

Areas Covered:

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 will 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

  • Registration Options


    Avail 12 months unlimited access for a single user.


    Material shipped within 15 days post webinar completion & get life time access for unlimited participants.



    Speaker Details

    Todd Graham

    Todd Graham

    Biotech, Pharma

    Todd Graham , is a masters-level bench scientist and medical technologist with a host of experience in both the clinical diagnostics and biotechnology fields. He has work for a number of start-up firms in the clinical diagnostics and biotechnology industries, as well as worked for larger firms within both industries. 

    Refund Policy



    Participants/Registrants for our live events, may cancel up to 72 hours prior to the start of the live session and ComplianceTrain will issue a letter of credit to be used towards any of ComplianceTrain's future events. The letter of credit will be valid for 12 months.

    ComplianceTrain will process refund in cases where the event has been cancelled and is not rescheduled within 90 days from the original scheduled date of the webinar. In case if a live webinar is cancelled, participants/registrants may choose between recorded version of the course or a refund. Refunds will not be processed to participants who do not show up for the webinar. A webinar may be cancelled due to unavoidable circumstances, participants will be notified 24 hours before the scheduled start of the event. Contact us via email: admin@ComplianceTrain.com