Softgel Encapsulation

CSI produces softgel capsules on 12 production lines, three shifts per day, 5 days per week. Capteks production capabilities produce on average 200 million softgels per month. The Company operates out of the main location at 16218 Arthur St. Cerritos, CA 90703.

All products are produced in compliance with new FDA cGMP Standards, which became effective on June 25, 2009 (Became effective for all manufacturers, packers, labelers and holders of dietary supplements with 21 to 500 FTE employees).  Prior to June, the FDA had regulated the industry pursuant to the Dietary Supplement Health and Education Act (DSHEA) of 1994, treating the companies as ‘food processors’. Captek/Natutac has been and remains a long-standing member of Natural Products Association (NPA, formerly NNFA, is very active in the industry's development of quality standards) www.naturalproductsassoc.org.

Captek is currently NPA certified. In its softgel manufacturing process the Company utilizes automated blending, forming, cooling, dehydrating and printing machines. The Quality Control (QC) and Quality Assurance departments are actively involved throughout all stages of the manufacturing process. Vendor certification of materials is required. In-house scientists in QC test all raw materials received based on current GMP standards. All formulated products and gelatin are blended in a clean room blending facility. All products are tested by in-house laboratory staff. Samples of all products produced are collected and tested. These processes insure proper seal, formulation, color, texture, and fill volume to insure your label claims are accurate.