Risk factors or compliance issues due to PCR assays

Date : 21st January 2020 to 21st November 2019

Place : United States, Newark

Website :http://bit.ly/2Nmkvqk

Contact Person:+1-(510)-868-1040

Description:

OVERVIEW A polymerase chain reaction is a powerful tool with a 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. LEARNING OBJECTIVES Reagent and consumable handling Proper set-up of a pre-PCR space Handling of template and various strategies to mitigate contamination Post-PCR set-up Analysis of PCR data to determine sources of issues Environmental concerns for PCR lab set-ups WHY SHOULD YOU ATTEND This webinar will help you get better peace of mind when it comes to the reliability of PCR assays, reducing the risk of quality, or regulatory issues. WHO WILL BENEFIT? This topic applies to personnel/companies in any laboratory that uses PCR. The employees who will benefit most include: Senior Management Quality Assurance Research and Development Environmental Services in laboratory facilities SPEAKER Todd 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, Todd 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. He has written several 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. For more detail please click on this below link: http://bit.ly/2Nmkvqk Email: [email protected] Tel: +1-(510)-868-1040

Risk factors or compliance issues due to PCR assays will be held in Newark,United States on date 2019-11-21

---

Deadline for abstracts/proposals : 21st January 2020

Keynote Speakers :

Venue :Online

Check the event website for more details.