Meeting with worldwide regulatory authorities (programs, study designs and submissions)
Training programs, technicians, study directors, QA/GLP's & Regulatory Affairs
Employee Safety Programs, OHSP
Facility design & AAALAC accreditation
Scientific and technical support
MSDS preparation
Review, write, edit draft reports and regulatory documents
Prepare report summaries
Preparation of SOPs & QA programs
Experience
Dr. Tierney has more than 30 years of experience in the life sciences industry, including 15 years CRO experience where he served as Director of Research, Associate Director of Toxicolog and Study Director for more than 300 pre-clinical safety evaluation studies of all types, in all species by all routes of administration. Tierney & Associates has performed extensive work in drug development in the U.S. and Asia for worldwide regulatory authorities in addition to establishing training programs for technicians, study directors, QA, GLP's and AAALAC. Extensive experience in writing reports, regulatory submissions and auditing pre-clinical studies and CRO's.
