EMINENT is committed to providing a complete range of quality Investigational Drug Management and InfoTech Services to the Pharmaceutical & Biotechnology Industry and Research Organizations in a very cost effective and timely manner.
EMINENT offers specialized regulatory guidance throughout the drug development cycle, from bulk drug characterization & formulation, cGMP manufacturing of clinical trial materials, to product launch.
All EMINENT operations are performed in strict compliance with current Good Manufacturing Practice (cGMP) regulations and a comprehensive body of Standard Operating Procedures with required permits and licenses.
The Pre-EMINENT provider of Pharmaceutical, Biological and Infotech Services