Multi-Matrix Full Chelate Cyto Matrix

Why Choose Cyto-Matrix? We are 100% committed to helping you improve lives. Cyto-Matrix's products The excellent clinical results that are achieved with our products, combined with our honest and ethical approach, has earned Cyto-Matrix the trust of many of the most scrutinizing Canadian health care practitioners. We are appreciative and honoured that new clients of Cyto-Matrix quickly become loyal clients and are open to building a lasting relationship with us. Our philosophy is simple; purity, integrity, innovation: Purity Products are developed using the highest grade possible raw materials with vegetable capsules while minimizing the use of excipients. All products are manufactured in state-of-the-art, Good Manufacturing Practices (GMP)-compliant Canadian facilities, meeting or exceeding pharmaceutical and Health Canada standards. Third-Party tested with rigorous QA/QC. Integrity All formulations are researched and designed by Naturopathic Doctors based on Health Canada-approved, evidence based science. Products are fully licensed with approved Health Canada label claims. All associates are required to adhere to the high ethical standards of the organization. Customer Service Representatives will refer technical questions to staff doctors, with accurate, fast-as-possible turn around. Innovation Cyto-Matrix is continually researching and adding cutting-edge formulas to meet the unique and changing needs of your patients. Expertise and innovation are shared through seminars, blog articles and Practice Pearls to aid in professional development and continuing education. Regular feedback from practiticing professionals and our National Advisory Board is an integral part of our innovation. Do share your feedback and ideas! Quality Manufacturing Cyto-Matrix products are manufactured in state-of-the-art Canadian facilities in Quebec and Ontario. Cyto-Matrix's manufacturing facility These facilities hold valid Site Licenses as per the requirements of Health Canada's Natural Health Product Directorate. In accordance with these guidelines, sites must have procedures in place for distribution records and product recalls and for the handling, storage and delivery of their products. They must also demonstrate that they meet Good Manufacturing Practice (GMP) requirements. The Quality Assurance Department This department is responsible for the development of Standard Operating Procedures (SOP's). The main goal here is to ensure the integrity of the result of the finished product. All SOP's ensure compliance with GMP requirements. Other responsibilities include: Editing of protocols and installation, operation and performance qualification implementation Validation of HVAC, purified water and other systems Validation of production of lab equipment Validation of process including manufacturing/cleaning/sterilizing The Quality Control Department Quality Control is done throughout the manufacturing process to ensure that the finished product meets the pre-determined specifications for micro-biological and physiological criteria. Raw materials are specifically tested to ensure the highest level of quality. The Validation Department Working closely with the QA and QC departments, the Validation department ensures compliance with all regulations and industry standards. In particular, the main responsibilities of this department are: Editing of protocols and installation, operation and performance qualification implementation Validation of HVAC, purified water and other systems Validation of production of lab equipment Validation of process including manufacturing/cleaning/sterilizing Cyto-Matrix Inc. is dedicated to sourcing the highest quality of raw materials available on the global market. It is the combination of high quality raw materials and strictly adhered to GMP practices, which make Cyto-Matrix products of a superior class in the natural health products market.