L2 Consulting works with an international client base of life science industries in finance, business planning, M+A, program design, executional oversight and interim management. Scientifically, L2 has contributed to over 300 new drug clinical trial applications (preclinical), has raised over U$200m in new funding and has been pivotal in closing 6 mid-sized M&A’s in the industry (including execution of full due diligence) with deal values of up to US$50m. L2’s team of Associate Partners encompasses senior level expertise in clinical, preclinical, bioanalytical immunological, finance and business/corporate development.
As an Associate Partner in L2 Consulting, Michael Keherly, Ph.D. is a quality professional with over 13 years of experience in regulatory affairs (GLP, GMP, GCP, animal welfare), including providing guidance to both regulated service providers and sponsors. His specialties include conducting audits/inspections of contract research and manufacturing organizations on behalf of sponsors, assisting contract research and manufacturing organizations comply with applicable regulatory requirements and quality standards, and providing compliance and regulatory training using innovative problem-based and active- learning methodologies. His research background also provides a unique perspective on the application of quality systems to scientific research and services.
Michael Keherly Ph.D