We are experienced with the application of GLPs in facilities of varying types and sizes.  We have provided QA support and conducted audits in facilities ranging in size from a few employees to multi-national corporations.  These audits have been conducted in facilities throughout the United States, Canada, the United Kingdom and Europe.

Because of this experience, we understand that there are multiple ways to approach meeting the GLP requirements and achieve compliance.  Our assessments and advice draw on this experience with a distinctive ability to evaluate how each facility has implemented procedures to meet GLP requirements.

Our experience includes conducting inspections and audits of studies required to be compliant with Food and Drug Administration (FDA), Environmental Protection Agency (EPA) and Organisation for Economic Co-operation and Development (OECD) GLPs.

Principal consultant, Mary E. Lynn, has been working in the GLP regulated industry since 1988.  She has an M.S. degree and is a Registered Quality Assurance Professional in GLPs.

Learn More:

FDA Experience EPA Experience