Developmental and Reproductive Toxicology
Over 25 years of experience in the Developmental and Reproductive Toxicology (DART) field.
Senior Research Scientist with command of all phases of DART laboratory processes and experience in the pharmaceutical industry.
20 years of direct oversight and management as Study Director for in-house nonclinical studies and as Study Monitor for multiple studies conducted at Contract Research Organizations (CROs).
Expertise in fetal morphology evaluations in multiple species.
Trainer for DART investigators and junior scientists in fetal morphology.
One of the first accredited Assessors for the International Register of Fetal Morphologists (IRFM) in the United States, (Active Assessor status).
Experience in the evaluation and assessment of technical staff in fetal morphology of large/medium/small laboratories in the US.
Contact Us
873 US Route 1 South #1064
North Brunswick, New Jersey 08902
tes.olitan@taodart.com
732-718-9511
Areas of Practice
Project study monitoring of Developmental and Reproductive Development Toxicology (DART) studies (eg, Embryo-Fetal Development [EFD], Fertility and Early Embryonic Development [FEED], Pre- and Postnatal Developmental [PPND] studies) conducted at CROs
Input on study design and protocol generation
Overseeing all in-life and post in-life phases of the study
Data review, reviewing of reports from draft through finalization and Common Technical Documents (CTDs)
One of the first accredited Assessors for the International Register of Fetal Morphologists (IRFM) in the United States, (Active Assessor status).
Get in Touch
Expertise in the evaluation and assessment of technical staff in fetal morphology of large/medium/small laboratories in the US.