Experic is a contract development and manufacturing organization (CDMO) and clinical trial supply services company dedicated to revolutionizing pharmaceutical development, manufacturing, and clinical trial supply. Established in 2018, Experic offers a comprehensive suite of services, including process development, analytical and formulation development, clinical and commercial manufacturing, and clinical packaging and logistics. Specializing in challenging powders and inhalation products, our expertise encompasses tablets, pellets, capsules, and low-dose dry powder inhalation therapies.

Operating from our state-of-the-art, Class A cGMP facility in Cranbury, New Jersey, we manage the global delivery of high-quality products, even for expedited projects. Our team of industry leaders brings decades of experience in pharmaceutical product development and clinical trial supplies, ensuring strategic vision and execution for every project.

At Experic, we are committed to delivering innovative, client-focused services that accelerate the development and commercialization of life-changing therapies. Our flexible, customer-oriented approach addresses the growing needs of the biopharmaceutical industry, making us a trusted partner in bringing innovative products to market.