SCIENCE

The Contract Manufacturing Partner currently operates out of a modern state-of-the-art 15,000 square foot manufacturing facility designed specifically for the manufacturing of pharmaceutical and nutritional products. This facility is temperature and humidity controlled with a central dust collection system. It is a licensed under the Federal Drug Administration (FDA) and California State as a Drug and Nutraceutical manufacturing facility and is subject to all requirements to maintain those licenses.

Before a product is introduced, the R&D, quality assurance and legal departments review the safety and efficacy of ingredients, set specifications for raw materials and finished products, and assess potential legal or regulatory issues. The R&D process and department ensures product formulations are safe and efficacious to the standards that have been developed. The bulk of the Company’s success is attributed to its ability to develop, manufacture and market innovative products for both branded and private label applications.

NuTech Medical products through its contract manufacturing are manufactured in full compliance with the Good Manufacturing Practices (GMP) set by the Federal Drug Administration (FDA) of the United States, and NuTech Medical places strong emphasis on its quality control practices. NuTech Medical follows all F.D.A. stated procedures, which require that all raw materials be tested from the receiving stage and stored in a designated quarantine area until NuTech’s contract manufacturer Medical Quality Control Department approves them for use. Bulk materials are tested for physical characteristics, active ingredient content, and for contamination such as heavy metals and microbes.

As a quality supplier of Nutraceutical and pharmaceutical products, our strategy includes developing and maintaining strong working relationships with our wholesale customers. Our sales and marketing teams will work with known Nutraceutical and pharmaceutical brand companies to get our formulations and/or their company’s formulations into the best chains and hospitals throughout our target markets. We believe in providing all point of sale materials and working closely with our distributors to take advantage of their local expertise in designing marketing and sales materials in there given geographic regions. We also rely on our long-term relationships in these market segments by the company’s founders and its Medical consultants that represent the highest quality of professionals in the medical industry with lifelong relationships at the highest level of management in our target markets.

The Federal Drug Administration (FDA) has the express responsibility to regulate the manufacturing process of Nutraceutical supplements. It issued its first proposed rule in 2003. In June 2007, it issued its final rule requiring all Nutraceutical supplement manufacturers to ensure by June 2010 that production complies with the current Good Manufacturing Practices (GMPs) similar to those of the pharmaceutical industry.

The FDA 21 Code of Federal Regulations (CFR) Part 111 was established to insure the identity, purity, quality, strength, and composition of Nutraceutical supplements and applies to those involved in the manufacture, packaging, labeling or holding of Nutraceutical supplements.