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Quality Control with Molecular Diagnostics

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Course Description:

This 1-hr virtual seminar will teach the key issues behind sample quality control for molecular diagnostics.

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.

Why should you Attend?

This webcast 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.

Areas Covered:

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
  • Challenges unique to PCR assays
  • Challenges unique to DNA fluorescent assays
  • Challenges unique to NGS assays

Who will benefit?

This will benefit a wide array of professionals such as:

  • Quality control
  • Assay Development
  • Assay validation
  • Research and Development
  • Clinical Diagnostics

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