Overview of Bioanalytical Method Validation

Event Information
Product Format
Prerecorded Event
Presenter(s)
Conference Date
Wed, Jan 18, 2017
Length
60 minutes
Product Description

Employing an Effective Bioanalytical Method Validation System


Bioanalytical method validation process includes several procedures, which depict that a particular method that is applied for quantitative measurement of the analytes in a given biological matrix like blood, plasma, serum, or urine, is completely reliable and reproducible for use as intended. It is necessary to employ properly-characterized and fully validated bio-analytical mechanisms to yield reliable results which can be interpreted satisfactorily.

Join expert speaker Edward F. O’Connor, PhD in a live webinar to gain better understanding of similarities and differences in the validation of LC, ligand binding, and cell based and other instrumental assessment approaches.

Session Highlights

  • Is the method ready for validation?
  • Column and plate considerations
  • Understanding specificity approaches
  • Review concomitant meds
  • Carrying out performance evaluations

Who should attend

The following personnel in bio-analytical laboratories

  • Analysts
  • QA Members
  • Supervisors
  • Managers

At the Q&A session following the live event, ask a question and get advice unique to your situation, directly from our expert speaker.

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About Our Speaker

Edward F. O’Connor

Edward F. O’Connor,Ph.D. has over 26 years of experience in GLP, GMP and GCP Analysis. He also has dealt extensively with GC­MS (FID, ECD, NPD), LC (MS, UV, FL, LSD, CL, COUL, CON), Plate Based Assays­ ELISA (UV, COL, CL, FL), MSD, Radiometric static and column, In Situ Hybridization of nucleotides, Cell based assays EC50. He also holds mastery of Compliance and Validation Issues. Edward has Directed, Supervised...   More Info
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