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SERVICES » Pharmaceutical Development » Stability
The ABC Difference

 

Pharmaceutical Development

Biotech Services-Recently Expanded!

DMPK and Bioanalytical Solutions (GLP)
Method Development & Validation
In-vitro DMPK Services
In-vivo DMPK Services
Bioanalytical Testing

Radiolabeling & Synthesis Solutions
non-GMP Services
CGMP Services
Phase 0 Development Support

CMC & QC Solutions (CGMP)
Method Development & Validation
Extractables/Leachables Studies
Trace Analysis & Structural Chemistry
Stability Programs and Release Testing

Drug Development Consulting

Environmental Assessments

Seamless Project Management
through Strategic Partnerships

Stability Programs & Release Testing

ABC Laboratories offers complete stability program management in support of IND, clinical, registration stability and post-marketing programs. We offer a secure, DEA-licensed stability suite that covers all ICH conditions, as well as photostability and custom conditions—with over 43,000 cubic feet of stability storage space.

A fully validated Rees monitoring system, redundant chamber systems, and 100% backup power supply ensure an optimally controlled, fully compliant CGMP environment for QC testing and sample storage. Our QC chemists work closely with the QA group to ensure rapid turnaround of accurate, QA-reviewed data.

Storage Conditions

  • 25 °C / 60% RH
  • 30 °C / 60% RH
  • 30 °C / 65% RH
  • 40 °C / 75% RH
  • -20 °C, 5 °C, 50 °C
  • Controlled Room Temperature
  • Special Requested Conditions
  • Photostability

Physical Testing

  • Color Determination
  • Container Closure Integrity
  • Deliverable Volume
  • Particle Size
  • Appearance
  • Loss on Drying
  • Disintegration
  • Melting Point
  • Boiling Point
  • Density
  • Friability
  • pH
  • Turbidity
  • Viscosity
  • Moisture
  • Osmolarity
  • Hardness
  • Particulates
Stability Suite

Our "phase-appropriate" approach to stability study design will help move your development program forward without unwarranted delays or expense.