Supplement Manufacturer 






Enzyme Process has the experience not easily found in the supplement manufacturing industry. Our professional and manufacturing staff average over 20 years of industry experience. The professional staff has the expert knowledge to help you formulate your next product. Our experience lets us recognize potential problems with your formula and any production issues before manufacturing begins saving you time and money. We also provide our clients with a supplement facts panel and guidance in the wording of the discussion panel that meets current FDA requirements. 

Our Manufacturing Facility

Enzyme Process is your FDA registered and inspected, cGMP certificate manufacturer of choice to make capsules, tablets chewable wafers, oral dissolving tablets and powders. When you choose Enzyme Process as your manufacturer, you have access to our temperature and humidity controlled state of the art 25,000 sqft facility.

What do we manufacture?

  • Capsules
  • Tablets
  • Powders
  • Chewable Tablets
  • Oral Dissolving Tablets

Our Quality

From blending to finished product all manufacturing takes place in an enclosed room with full vacuum and particulate collection. These steps ensure there is no cross-contamination. Enzyme Process maintains a full analytical laboratory to test for identity, potency and microbiological contamination from a raw material and manufacturing stage to finished product. Having an analytical laboratory in-house reduces cost and saves our clients money. 

Enzyme Process Guarantees to our clients the following: 

     - Your Product will meet or exceed label claims. 
     - Your product will be free of Mold, Yeast, E.coli, Staph Aureus & Salmonella
     - Certified of Analysis provided with every order. 
     - cGMP certificate available upon request. 

Enzyme Process is the obvious choice to bring your next dietary supplement idea to market. Contact us today to get started!

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