Invitron provides stability testing and stability storage support to the pharmaceutical industry. We conduct ICH stability studies following client supplied methods, compendial methods or methods that have been developed and validated by our own analysts. Stability testing for virtually all types of drug formulations including, but not limited to, sterile injectable products, tablets, capsules, non-sterile liquids, transdermal products, aerosols, and medical device combination products are performed at our site. We support long and short-term (accelerated) stability programs as well as photostability programs for Research & Development and commercial products. Our stability storage chambers are fully mapped and continuously monitored by a validated, continuous monitoring system. Our chambers and monitoring system are supported by external back-up power generators in the event of any power failure.


We offer the following ICH stability storage conditions and client specific storage conditions:

  1. Total storage capacity 80k liters
  2. 25°C ± 2°C / 60% RH ± 5% RH
  3. 30°C ± 2°C / 65% RH ± 5% RH
  4. 40°C ± 2°C / 75% RH ± 5% RH
  5. 40°C ± 2°C / 25% RH ± 5% RH
  6. 5°C ± 3°C
  7. 25°C ± 2°C / 40% RH ± 5% RH
  8. -20°C ± 5°C
  9. Photo Stability Study
  10. Continuous Monitoring and Emergency Power Systems