At Innovotech, we conduct stability testing to help clients determine the shelf life, safety, and performance of their regulated products. Our team designs and manages real-time and accelerated stability studies under controlled environmental conditions to meet Health Canada, ICH, and WHO guidelines. Using validated environmental chambers and precision monitoring systems, we ensure your product data is reliable, compliant, and ready for regulatory submission.
Our services help manufacturers in the pharmaceutical, medical device and and Natural Health product industries understand how temperature and humidity affect product integrity—supporting decisions on formulation, packaging, and storage requirements.
Our validated chambers maintain 25°C / 60–65% RH for real-time and 40°C / 75% RH for accelerated testing. Custom conditions are also available.
Typical real-time studies run for 12 to 24 months, while accelerated testing can generate predictive results within weeks.
Yes. Our experts collaborate with clients to define test parameters, pull points, and analytical methods tailored to product specifications.
All data is collected under GMP-compliant systems, with traceable documentation and continuous chamber monitoring to ensure study integrity.
Yes, our team can assist with meeting the client’s specific testing needs to determine for physical, chemical and microbiological changes that would impact product quality, safety and efficacy.
