 Cytozyme Laboratories, Inc. is dedicated to supplying products of the highest industry standards. We follow guidelines of Good Manufacturing Practices and Total Quality Management programs. Our employees are trained to adhere to strict manufacturing procedures and to continually focus on quality during each step of the manufacturing process.
Each batch of product, identified by a unique lot number, undergoes rigorous, multi-step quality assurance procedures performed by several departments and thoroughly outlined in our Standard Operating Procedures. Product quality assurance starts with the purchasing of raw materials and continues through manufacturing, packaging, shipping and distribution processes. To guarantee the quality of our products, Cytozyme Laboratories, Inc. keeps samples and records of each batch of product for a minimum of five years.
Our Quality Control Department ensures that each product complies with the diverse requirements of State and Federal Departments of Agriculture and other Regulatory Agencies responsible for evaluating and registering products both domestically and internationally.
The director of our Quality Control Department ensures that the analytical procedures follow stringent scientific principles that require in depth knowledge of analytical and regulatory topics. The testing is performed following Good Laboratory Practices and utilizing Official Methods developed and approved by AOAC International. Each finished product manufactured by Cytozyme Laboratories undergoes rigorous quality control procedures, including detailed physical and chemical analysis. Products are additionally tested for biological activity using proprietary bioassay procedures designed to ensure uniform performance
of each product batch in the field. The Analytical Quality Control Director reviews all analytical test results and certifies the quality of each batch of product.
 Quality Guidelines
Cytozyme Laboratories, Inc. follows GMP, FDA, GLP, AOAC, NASC and ISO guidelines.
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