Vitamin Manufacturer since 1950's
The effect of enzyme rich nutritional supplements on health was noticed back in the 1950's. At the time, Dr William Hanson, a brilliant young scientist and founder of Hanson Research, developed methods of enzyme extraction to preserve the life sustaining substances in food extracts. In 1988 David Roderick, whose service in the nutritional supplement industry dates back to the late 1950's, purchased Enzyme Process Laboratories. Under his guidance, Enzyme Process began marketing their blend of unique and proven products into the nutritional arena. The combination of nutraceutical herbs with vitamins, minerals, alkalizers and enzymes gives Enzyme Process products a spectrum of supplements that are unequaled in efficacy, safety and marketability. Each product is produced using an enzymatic process extraction to maximize the dissolution and absorption of its nutrient concentration. This process is what separates Enzyme Process products from all the rest. We specialize in custom formulations, specialty products and private labeling. Our Facility:
Enzyme Process conducts its contract manufacturing to assure consistent, efficient production, within shortlead times to meet desired specifications. You can be certain that Enzyme Process will manufacture your tablets, capsules, and powders according to your specifications and will perform appropriate quality assurance tests throughout the entire manufacturing process. Enzyme Process' turnkey facility is equipped to provide the highest quality nutritional and dietary supplements available. All of our manufacturing rooms are temperature controlled, enclosed with full vacuum and particulate collection equipment in place. These techniques ensure quality and avoid cross contamination.We apply the most current research and technology to help our clients create innovative products that meet or exceed their production and development objectives, including custom orders and special requests. Enzyme Process' dedication to superior quality guarantees an extra level of quality assurance. Rigorous quality assurance measures include quarantining all raw materials until composition, identity, and integrity are confirmed and full documentation provided according to the FDA cGMP standards we observe. Our facility is inspected monthly to ensure cleanliness and safety guidelines are followed. Thorough materials analysis, visual inspection, and laboratory validation ensure only those products that meet the highest standards for purity, potency and efficacy are released for manufacturing and distribution. Only raw materials that meet or exceed our quality requirements are then purchased. Once the procured material arrives at our facility they are held until our quality assurance and quality control teams re-validate the product for identity, purity, and strength.
