Aizant offers complete stability testing programs on pharmaceutically relevant compounds including API’s, pilot-formulation, packaging changes, drug development, customer manufactured products, clinical trial supplies and current marketed products. All storage conditions are validated, monitored in compliance with 21 CFR Part 11.

We offer:

	Stability protocol design including bracketing and matrixing
	Storage of stability samples as per ICH guidelines include long-term, intermediate and accelerated testing
	Storage of stability samples under custom conditions including reconstitution study, freeze-thaw cycle, photo stability, temperature, etc.,
	Transfer of customer validated methodology to our laboratories