Selection of Contract Research Organizations (CROs) to Support GLP, GCP and GCP Bioanalysis

Event Information
Product Format
Prerecorded Event
Conference Date
Thu, Apr 20, 2017
60 minutes
Product Description

How to Select CROs to Support GLP, GCP, and GCP Bioanalysis?

Selection of a Contract Research Organization (CRO) to support non-clinical and clinical bioanalytical is complex and involves more than cost and proximity considerations.

Join this session by expert speaker Edward F. O’ Connor, Ph.D., where he will outline the process and the considerations necessary to minimize the risk of non-compliance, missing timelines, scope creep (and corollary extensions of timelines and budgets).

Session Highlights

  • The identification and selection process to minimize risk
  • Technology Considerations
  • On-site audits
  • Keeping Score
  • Keeping the playing field level—Use of WEBEX or similar for presentations
  • Reducing opportunity for failure, good communication
  • Processes including non-disclosure agreements, RFP, Presentations
  • Considerations of LAB movements or acquisition on project
  • Table of CRO comparisons and objective ratings for selection
  • Reagent considerations
  • Communication including format, frequency

Who Should Attend

  • Outsourcing Managers
  • QA auditors
  • Principal Scientists
  • Program and Study Directors

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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
More Events By The Speaker

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