About Us

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EXPERIENCED NONCLINICAL STUDY MONITORS, AUDITORS AND STUDY MANAGERS

The TOXPLUS Team has decades of experience and extensive knowledge of the drug development process including regulatory compliance requirements, nonclinical studies involving all species of animals, routes of exposure, and frequency of dosing as well as type of molecule being developed.

MEET THE PRESIDENT

Angela Lynch

Angela Lynch, MSPH, PhD, DABT

Angela Lynch has more than 30 years of research, consulting, and regulatory experience.

Angela Lynch, MSPH, Ph.D., DABT

Angela Lynch has more than 30 years of research, consulting, and regulatory experience. She is a pharmacologist and toxicologist, who has extensive experience with both big and small companies within the biotech and pharmaceutical industries. Angela has relationships with national and international CROs.

She has expertise with small molecules, biologics, as well as gene therapies in developing protocols, study monitoring, reviewing, and summarizing both GLP and non-GLP nonclinical pharmacology. She is also proficient in toxicology data, as well as other published scientific data of various types of pharmacology and toxicology study types.

She also has experience interacting with regulatory agencies and regulators. She is an active member of the American College of Toxicology, Society of Toxicology, and Regulatory Affairs Professional Society and a Diplomate of the American Board of Toxicology (DABT).

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