COMPANY INFORMATION
Biosynergy, Inc. was incorporated as an Illinois corporation on February 9, 1976. The Company's products utilize cholesteric liquid crystals, which are semi-synthetic esters of cholesterol and organic acids. It presently has 8 disposable devices utilizing five basic technological concepts including cholesteric ester time temperature phase technology and 2 other devices available for sale in the above-described markets.
 
MANUFACTURING/EXPERIENCE
The Company manufactures substantially all of its products except the HemoTemp® II Activator and Hemo-CoolJr II. These devices are manufactured exclusively for the Company by unrelated companies on an as-needed basis. Raw materials for the Company's other products are purchased on an as-needed basis, and assembly of the products is performed at the Company's production facility. Biosynergy, Inc. has 30 years of experience working with various liquid crystal formulations and application methods. The Company maintains complete records of manufacturing and quality assurance testing of all of its products in compliance with Food and Drug Administration ("FDA") regulations. All products are manufactured according to "good manufacturing practices" (GMP) for medical devices.
 
Q.C. PRODUCTS ASSIST IN COMPLYING WITH FDA/AABB GUIDELINES
Biosynergy, Inc. has designed its quality control products, such as HemoTemp® II, to assist end-users in complying with FDA and AABB guidelines for temperature control during shipment and storage of human blood and other biologicals.
 

COMPANY MISSION STATEMENT
Biosynergy is presently engaged in the development, production and marketing of thermometric, thermographic and thermoelectric products designed for quality control purposes to be used in the medical, laboratory, industrial and food markets. Our Mission is to provide the highest quality products to all of our customers while maintaining complete records of manufacturing and quality assurance testing of all of its products in compliance with Food and Drug Administration ("FDA") regulations. Biosynergy, Inc. has 30 years experience working with various liquid crystal formulations and application methods and all products are manufactured according to "good manufacturing practices" (GMP) for medical devices.


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