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).
Who Should Attend
- Casper E. Uldriks
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...
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