Sample Quality Control for Molecular Diagnostics

Duration: 60 Minutes
In this webinar attendees will learn the key issues and sample requirements (collection methods, sample inhibition and sample volume) for molecular diagnostics and the tools (PCR, DNA fluorescent assays & NGS assays) you need to deal with your laboratory challenges in clinical laboratory.
Quality Control for Molecular Diagnostics
Instructor: Todd Graham
Product ID: 507069
Objectives of the Presentation
This webinar will help you learn how to deal with sample quality control for molecular diagnostics. The webinar will include the following critical information you will need:
  • Universal sample requirements for molecular diagnostics
  • Strategies to deal with common challenges
  • Challenges unique to PCR assays
  • Challenges unique to DNA fluorescent assays
  • Challenges unique to NGS assays
  • Challenges unique to newer molecular technologies
Why Should you Attend
Since the beginning of the PCR revolution in the 1980s, molecular diagnostics have proven to be a useful tool for the clinical laboratory. The ability to analyze a variety of samples for DNA and RNA content have proven to be useful for a large number of clinical conditions using a number of different technologies. However, each technology has its pitfalls with how to handle samples for optimal results. In addition, different technologies have different challenges as to what can inhibit optimal results, and each technology has a unique solution to these pitfalls.

This webinar explains a variety of issues and how to address them. Common issues such as collection methods, sample inhibition and sample volume will be address. Also, each unique technology, from standard PCR, to DNA fluorescent assays, from next generation sequencing to newer technologies such as point of care and digital PCR, will have their various sample challenges addressed. This webinar will give you the tools you need to deal with your laboratories challenges.

Who will Benefit
  • Quality control
  • Assay Development
  • Assay validation
  • Research and Development
  • Clinical Diagnostics
$200
Recorded Session for one participant
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  $250.00 Training CD
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  $300.00 Training USB Flash Drive
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How it works
Live Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • The webinar joining link, username and password for joining the webinar will be updated on your OCP Account 24 hours prior to the webinar
  • 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
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • 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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