Method development & validation
Vetio is fully equipped to develop chromatographic and spectrophotometric pharmaceutical analytical methods for determination of assay, dissolution, and related substances in various drug products. Our analytical methods are validated in a laboratory fully aligned with current Good Manufacturing Practices (cGMP) and ICH guidelines.
Drug product release testing
Our experienced scientists and state-of-the-art equipment afford efficient and quality release testing services. This service is offered as a standalone contract offering. Products tested in our Health Canada and FDA-approved Montreal facility allow for product release to multiple markets through mutual recognition agreements.
VICH stability studies
Vetio has the analytical resources and expertise to perform pre-commercial and commercial product stability testing. Other studies performed include forced degradation, statistical analysis, data trending, drug product comparison stability testing, and photostability.
We offer walk-in and reach-in stability chambers with ample product storage space across two physical locations with a range of temperature and humidity conditions. Each stability chamber is continuously maintained and monitored, including secondary power supply. We offer the following storage conditions:
- 25 °C – 40 °C (55 – 75% RH)
- 25 °C (60% RH)
- 30 °C (65% RH)
- 40 °C (75% RH)
- Ambient humidity
- -20 °C, -4 °C, 5 °C, 30 °C, 40 °C
No matter the issue—product, process, development, manufacturing, packaging, or technology transfer related—we’re driven to solve specific animal health problems with our customers.
How can we help you?
Please contact us and let us know how we can leverage our animal health knowledge and CDMO proficiency to help you actualize animal health.