HartmannWillner LLC offers services to the FDA-regulated industry that span the development process to include preclinical and nonclinical development (pharmacology/toxicology); clinical; chemistry, manufacturing and controls (CMC) and quality; and compliance with GLP, GCP, GMP, GCLP, and CLIA.

Additional information may be found at:

Regulatory Affairs


Biopharmaceutical Development

Strategy, Management and Leadership

Agent Services