Validation of Lonza Facility; Utilities and Equipment. Lonza shall maintain cGMP validation status of the Lonza Facility, as well as the utilities and equipment used in the manufacture of Bulk Drug at the Lonza Facility, and shall make relevant validation reports applicable thereto (which may be redacted to remove information not related to the manufacture of Bulk Drug) available to Trubion for review at Lonza's Facility, at Trubion's reasonable request.
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Samples: Manufacturing Services Agreement (Trubion Pharmaceuticals, Inc), Manufacturing Services Agreement (Trubion Pharmaceuticals, Inc), Manufacturing Services Agreement (Trubion Pharmaceuticals, Inc)
Validation of Lonza Facility; Utilities and Equipment. Lonza shall maintain cGMP validation status of the Lonza Facility, as well as the utilities and equipment used in the manufacture of Bulk Drug at the Lonza Facility, and shall make relevant validation reports applicable thereto (which may be redacted to remove information not related to the manufacture of Bulk Drug) available to Trubion Genentech for review at Lonza's Facility, at Trubion's Genentech’s reasonable request.
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