With over 14,000 ft2 storage capacity and over 14 ICH and custom conditions, Avecia Pharma has the capability to help design stability studies tailored to product needs.

Partner with Our Stability Testing Team

For the quality control and security your projects demand, all CGMP validated environmental and photostability chambers are monitored 24 hours a day by a computer-based Environmental Monitoring System. Our walk-in, reach-in, UV/visible and fluorescent photostability chambers are supported by back-up chambers, a reserve generator and an electronic notification system.

We have the latest Stability Laboratory Information Management System (LIMS) to ensure compliance. The system accommodates sophisticated sample management, as well as allows the stability department to generate cumulative reports.

At Avecia Pharma, our mission is to provide our clients with outsourcing solutions that make their drug development priorities possible.

Providing High Quality Testing & Reliable Storage

  • Clinical
  • Commercial
  • NDA
  • BLA
  • ANDA
  • IND

Comprehensive Stability Studies & Services

  • Stability protocol generation
  • Stability testing
  • Stability storage
  • Stability summary report generation
  • Stability time points and conditions specific report generation
  • Freeze/ thaw studies
  • Stability time points and conditions specific report generation
  • Preclinical stability
  • Clinical stability
  • Stability indicating method development and validation
  • Release testing
  • Method transfer and analyses qualification
  • Assay, impurities, dissolution, water content, etc. of various formulations

Range of Storage Conditions

  • 25°C/60% RH
  • 30°C/65% RH
  • 40°C/75% RH
  • 25°C/40% RH
  • 40°C/25% RH
  • 25°C
  • 50°C
  • 60°C
  • 5°C, Refrigerator
  • -20°C, Freezer
  • -40°C, Freezer
  • -70°C, Ultimate freezer
  • Photostability chambers – ICH options I and II
  • Customized conditions
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