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 to product launch.
All operations of EMINENT are performed in strict compliance with current Good Manufacturing Practice (cGMP) regulations and a comprehensive body of Standard Operating Procedures.
A well planned clinical study is the key to the success of any emerging pharmaceutical or biotechnology company. EMINENT is the ideal partner to assist the pharmaceutical & biotechnology industry in dealing with the regulatory issues, cGMP issues, study product development, and information management and technology components of clinical studies.