How to Translate Academic and Discovery Assays into GLP Compliant Assays

Duration: 60 Minutes
This 1-hr virtual seminar will help you deal with the challenges and pitfalls that may occur when translating assays as demonstrated in the scientific literature or through internal discovery efforts. While academic research needs only to be novel, interesting and scientifically sound to be published, there may be gaps in the known information about the assay to allow it to go into production use, either for internal industrial research laboratory efforts, clinical trial usage or even for use as a diagnostic assay. This assay will help you learn what needs to be done to sheperd any given assay from the academic world to the industrial world.
GLP Compliance
Instructor: Todd Graham
Product ID: 500247

Why Should you Attend:
Every day, there are a number of novel and interesting discoveries that are published in the academic literature. Many of them, if proven to be true, will lead to improved industrial research and potentially improved human health. However, there is a dramatic difference in documentation standards between the academic world and the industrial world, and learning how to bridge that gap successfully will require strong investigational skills to find out what truly happened during the performance of the assay and the conditions therein needed to perform it. After this seminar, you will be able to fill in the gaps with confidence and learn what you need to find out to sheperd key discoveries between worlds to ultimately further the goal of the biotechnology and pharmaceutical industries of improving human life.

Objectives of the Presentation:
This webinar will help you identify the key steps needed to be taken while transitioning a new assay from the academic world to the industrial world. The webinar will include the following critical information you will need:
  • What to look for in lab books and other notes to see what was performed
  • How to ask academic scientific staff for other key information they may not realize is important
  • How to determine whether a test is feasible for industrial usage, regardless of the technical validity of the test
  • How to track down controls, reagents and test appartus and test them using existing methods for suitability and quality
  • How to develop the necessary reagents needed to perform the assay in an industrial context
  • What kinds of repetition and repeatability studies are typically needed
Who can Benefit:
This topic applies to personnel / companies in the biotechnology and pharmaceutical industry. The employees who will benefit most include:
  • Senior management
  • Quality Assurance
  • Research and Development
$375
Recorded Session for one participant
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  $500.00 Training CD
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  $600.00 Flash Drive
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Minimum 10 attendees
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Live Session - How it works
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  • 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
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  • 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.


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