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Todd B. Graham

Biotechnology Professional, Clinincal Laboratory technology

Todd B. Graham is a clinical laboratory scientist for a large hospital system in the New York Tri-State Area as well as a scientific consultant for Fortune 500 biotechnology firms, healthcare systems throughout the world and R1 Research Level Universities. During his time as a clinical laboratory scientist in his current role, he has improved sample workflow and improved laboratory quality and sample turnaround time while expanding laboratory services to vulnerable health populations in the New York area. He has also provided outreach to the local community by serving as a mentor to students training in clinical laboratory science, as well as the scientific community by serving as a technical resource for his peers in the laboratory.

Through his work as a consultant, he has worked to improve the spread of key technical information in a variety of mediums. Todd has written a number of market research reports used by Fortune 500 biotechnology firms in strategic planning, and led webinars on key quality issues that impact the biotechnology community. He has served R1 Research Level Universities by advising them on strategic technology transfer opportunities, and has been called upon as a key knowledge leader internationally for the biotechnology industry.

Todd Graham graduated in 2006 with a MA in Biology at Queens College (City University of New York) after conducting published research in Molecular Evolution in the laboratory of Dr. Stephane Boissinot. He graduated as a Dean’s List student and James Dickson Carr Scholar from Rutgers University in 2001 with a BS in Biotechnology, where he continues to mentor Biotechnology students. He is a member of the Society for Laboratory Automation and Screening. He is also licensed as a Clinical Laboratory Technologist in New York State and is certified in Molecular Diagnostics by the American Society for Clinical Pathology.



  •  Wednesday, March 20, 2019
  • 10:00 AM PDT | 01:00 PM EDT,
  • 60 Minutes
  • ¤150.00
Effective Ways to Prepare a Standard Operating Procedure (SOP) : Writing, Updating and Maintaining Compliance

Standard Operating Procedures (SOPs) are required for companies that are regulated.

  •  Wednesday, April 17, 2019
  • 10:00 AM PDT | 01:00 PM EDT,
  • 60 Minutes
  • ¤150.00
SOP's for Bioanalytical Methods Validation

The webinar will include the following critical information

  •  Friday, May 3, 2019
  • 10:00 AM PDT | 01:00 PM EDT,
  • 60 Minutes
  • ¤150.00
Quality Control for Microbiological Media and Reagents

This webinar will help you develop a quality control program that fits your microbiological laboratory's needs.





  • Recorded
  • View Anytime
  • 60 Minutes
  • ¤190.00
Effective Ways to Prepare a Standard Operating Procedure (SOP) : Writing, Updating and Maintaining Compliance

Standard Operating Procedures (SOPs) are required for companies that are regulated.

  • Recorded
  • View Anytime
  • 60 Minutes
  • ¤190.00
SOP's for Bioanalytical Methods Validation

The webinar will include the following critical information

  • Recorded
  • View Anytime
  • 60 Minutes
  • ¤190.00
Quality Control for Microbiological Media and Reagents

This webinar will help you develop a quality control program that fits your microbiological laboratory's needs.