Velesco has partnered with Stability storage provider Vindonwestech, Inc. to enhance its drug formulation development program and clinical trial manufacturing services.

Velesco supports early stage drug development projects from two locations in Plymouth and Kalamazoo, MI with contract analytical and drug formulation services, as well as cGMP clinical supplies for non-sterile dosage forms. Vindonwestech, Inc. provides services for both CROs and pharmaceutical manufacturers, facilitating cGMP storage of biological and pharmaceutical materials over a wide array of temperature and humidity.

Vindonwestech also designs, manufactures and installs a wide range of standard and custom controlled environment room systems, validated to meet the demanding requirements of the pharmaceutical, medical, biological and healthcare industries.

Patrick Jackson, director of Vindon, commented, “Vindonwestech is pleased to be associated with Velesco as Vindonwestech is particularly committed to providing storage services and equipment strengthening Velesco’s ability to deliver a first class stability program.”

Shirley Smith, Quality Assurance director at Velesco noted, “the Vindonwestech facility is impressively designed and equipped. A Velesco and Vindonwestech collaboration assures a strong cGMP quality program and clients can be confident their clinical trial materials will exceed FDA Compliance requirements.”