Analytical Services: Solutions For Every Testing Need

Potent, cytotoxic, and DEA-controlled formulations leave little room for error in analytical work, and every method transfer or added vendor introduces another point of risk. This fact sheet outlines how an FDA- and DEA-registered laboratory, with 30,000 square feet of space and more than 300 scientists and support staff, supports drug products from Phase I through commercial supply. It details the instrumentation behind method development, validation, and release testing, along with specialized physical-functional work such as container closure integrity, dose accuracy, in vitro release, and dedicated photostability. It also describes how labs connected to aseptic and oral solid dose manufacturing keep data tied to the product.

Review the equipment list and capabilities to see how the model fits your program.