Todd Graham
Biotechnology Professional and Consultant
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.

Upcoming Webinar
Live Sessions Not Found.
Recorded Webinar
Sample Quality Control for Molecular Diagnostics
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.
Recorded Session Get life time access for one participant with download option!

SOP's for Bioanalytical Methods Validation
This webinar will help you learn how to validate bioanalytical methods. This session will teach you the pitfalls behind bioanalytical methods validation, allowing one to transition between assays with ease. This training on bio-analytical methods validation will help you understand the clear, consistent and compliant approaches for instrumental, ligand binding, and cell based methods. A comparison of EMEA and FDA guidance’s will be presented.
Recorded Session Get life time access for one participant with download option!

Quality Control for Microbiological Media and Reagents
This 1-hour virtual seminar will give you the tools you need to maintain a quality supply of media and reagents in a variety of microbiology laboratories. A thorough understanding of variety of challenges is necessary to maintain quality of the media and reagents will be brought to the fore. This will allow you to perform microbiology testing with confidence.
Recorded Session Get life time access for one participant with download option!

Transitioning Assays from Different Technologies - Validation and Qualification
This 1-hr webinar will help you understand the steps that must 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 and develop a transition plan to make sure results could be easily compared between the two technologies.
Recorded Session Get life time access for one participant with download option!

Risk factors or compliance issues due to PCR assays
Polymerase chain reaction is a powerful tool with wide variety of applications in laboratories. During the past 30 years, PCR has been used to accomplish a number of different tasks in biological research, clinical diagnostics, forensics and other tasks. The biggest issue is that the sensitivity of the technique could be a definite weakness in maintaining the quality of the assay. There could be Issues that may cause even the most well designed assay to have poor performance. This webinar will help pinpoint the steps in the PCR process that have the greatest risk, and the potential mitigation steps to prevent them. From subtle issues such as tube selection to pre-PCR set-up, from reagent selection to post-PCR handling, a wide array of issues will be dealt with to help improve the quality of PCR assays.
Recorded Session Get life time access for one participant with download option!

How to Translate Academic and Discovery Assays into GLP Compliant Assays
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.
Recorded Session Get life time access for one participant with download option!

How to Develop Quality Systems for New Diagnostic Assays
This 1-hr virtual seminar will help you understand the the necessary steps of develop a quality system for a new diagnostic assay that will comply with Good Laboratory Practices and Good Manufacturing Practices in the United States. The resulting quality system will support the develop of an assay for diagnostic use that can be approved through either the 510(k) process or the Pre-Market Application (PMA) process.
Recorded Session Get life time access for one participant with download option!

SUBSCRIBE TO NEWSLETTER
Get industry updates and exclusive deals on offers!