Meet the instructors

Employing the brightest minds in the life science industry

We believe the success of any training program begins with the selection of the right instructor. Simply put, we only hire the best in the business. Our trainers blend the right mix of subject matter expertise, instructional experience, and relevance in industry.

Dalfoni Banerjee

Principal Consultant & CEO, 3Sixty Pharma Solutions LLC

Dalfoni Banerjee is an award-winning, solution-focused entrepreneur. Beginning her career over 25 years ago in academic, pharmaceutical, and biotechnology research laboratories, she went on to lead inspection-readiness efforts, drive clinical research and clinical operations, manage relationships between pharma and key opinion leaders, develop marketing strategies/tactics, and launch new drug products – across 12+ therapeutic categories

Keith Dorricott

Clinical Process Improvement Expert

Expert in process improvement, metrics, and root cause analysis in clinical trials

Brooke L. Casselberry


Brooke Casselberry is the founder of Cyan Life Sciences, providing consulting services across the regulatory product lifecycle. Brooke’s experienced in developing regulatory domains, expanding business, and supporting clients in knowledge exchange, technology procurement and support, project management, and methodology development.

Natalee Kestler

Sales & Market Strategy Consultant

Natalee received her Nursing Degree from Union University and has practiced in the areas of Intensive Care and Surgery. She has a background in Sales and Sales Management in Home Infusion, Capital Equipment, Surgical devices and Biologicals.

Jerry Chapman

GMP Consultant

Jerry Chapman is a GMP consultant with nearly 40 years of experience in the pharmaceutical industry.

Greg Martin

Pharmaceutical Analytical Chemistry Expert

Greg Martin is President of Complectors Consulting ( which provides consulting and training in the area of Pharmaceutical Analytical Chemistry. Mr. Martin has over 25 years experience in the pharmaceutical industry and was Director of Pharmaceutical Analytical Chemistry (R&D) for a major PhRMA company for a number of years.

Lisa Olson

Part 11 / CSV Auditor, Polaris Compliance Consultants

Lisa Olson has over 30 years of experience in FDA-regulated industry, with a major pharmaceutical company, three CROs, and in consulting roles. With a background in system development and support of clinical research systems, she developed her career into regulatory compliance of computer systems and a specialization in 21 CFR Part 11.

Luisa Monica

Trial Master File expert

Luisa Monica’s experience includes oversight of electronic TMF (eTMF) implementation, quality control, coordination of migration projects, facilitated training programs, enhancement and development of TMF processes, and extensive inspection readiness preparation for FDA and MHRA inspections.