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.


  • Regulatory Consulting
  • Formulation and Development
  • Pharmaceutical Research
  • Clinical Manufacturing
  • Packaging and Labeling
  • Drug Repository
  • Direct-To-Patient (Rx)
  • Clinical Distribution
  • Clinical Randomization
  • Information Technology


  • FDA Registered Drug Establishment
  • Registered National Drug Code (NDC)
  • State Pharmacy License
  • State Pharmacy Distributor
  • State Controlled Drug Substance License
  • DEA Manufacturing/ Distribution/ Research/ Pharmacy
  • EPA Regulated Waste Disposer
  • State Special Medical Waste Disposer


  • 57,000 sft Free Standing Building
  • Uninterrupted Power (Two Backup Diesel Generators)
  • Redundant Equipments/Storage Units
  • 24/7 Temperature/RH Monitoring
  • Fire Detection/Suppression System
  • Disaster Recovery Plan
  • Offsite Data Servers/Back-up
  • Clinical Emergency Hotline, 24/7
  • Online Access to Reports/ Order Status/ Inventory

The Pre-EMINENT provider of Pharmaceutical, Biological and Infotech Services