15 May 1987
INTERIM COMMERCIAL ITEM DESCRIPTION
INSULIN, HUMAN, ZINC SUSPENSION,
100 U/ML, 10 ML
The General Services Administration has authorized the use of this Interim Commercial Item Description which was developed by the Defense Personnel Support Center, Directorate of Medical Materiel, DPSC-RST, 2800 South 20th Street, Philadelphia, PA 19101, based upon currently available technical information.
Shall be Insulin, Human, Zinc Suspension.
All ingredients shall be pharmaceutical grade.
Shall be delivered by Enzymatic Conversion of Human Proinsulin to Human Insulin.
Shall be a suspension containing 100 USP units per ml with less than 10 ppm of Human Proinsulin, within the applicable assay limits for the suspension.
Workmanship. The suspension shall be free from defects which detract from its appearance or impair its serviceability.
Unit. Vial (VI). Shall be supplied 10 ml in a commercially available multiple-dose vial, as specified, constitutes one unit.
Contractor certification. The contractor shall certify that the product offered meets the salient characteristics of this description and conforms to the producersí own drawings, specifications, standards, and quality assurance practices. The Government reserves the right to require proof of such conformance prior to first delivery and thereafter as may be otherwise provided for under the provisions of the contract.
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
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