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We are EMINENT
Services Corporation

Reliable partner for your clinical trials.

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.

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Commercialization

EMINENT offers specialized regulatory guidance throughout the drug development cycle, from bulk drug characterization & formulation, cGMP manufacturing of clinical trial materials, to product launch.
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Licenses and Permits

FDA Registered Establishment
NDC Labeler Code


EPA Regulated Waste ID

DEA Manufacturer | Exporter | Research | Pharmacy Registration

Maryland State Pharmacy Distributor License
Maryland State Pharmacy License
Maryland State Controlled Dangerous Substance
Maryland State Special Medical Waste ID

1

Commitment

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.
2

Commercialization

EMINENT offers specialized regulatory guidance throughout the drug development cycle, from bulk drug characterization & formulation, cGMP manufacturing of clinical trial materials, to product launch.
3

Compliance

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.

1

Commitment

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.

2

Commercialization

EMINENT offers specialized regulatory guidance throughout the drug development cycle, from bulk drug characterization & formulation, cGMP manufacturing of clinical trial materials, to product launch.

3

Compliance

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.

SERVICES
  • Regulatory Consulting
  • Formulation and Development
  • Pharmaceutical Research
  • Clinical Manufacturing
  • Packaging and Labeling
  • Drug Repository
  • Direct-To-Patient (Rx)
  • Clinical Distribution
  • Clinical Randomization
  • Information Technology
Discover our services
PERMITS
  • FDA Registered Drug Establishment
  • NDC Labeler Code
  • MD State Pharmacy License
  • MD State Pharmacy Distributor
  • MD State Controlled Drug Substance License
  • DEA Manufacturer | Exporter | Research | Pharmacy
  • EPA Regulated Waste ID
  • MD State Special Medical Waste ID
Review our permits
FACILITY
  • 57,000 sqft 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
Discover our facilities
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Donald Russel
AdvanceJoe
Since 1997

The pre-eminent provider of pharmaceutical, biological and infotech services

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