Our Standards of Operation Procedures (SOPS) are in compliance with the levels of pharmaceutical-grade and are based on the Good Manufacturing Practices (GMP), according to the documentation 21 CFR 111 of the United States Pharmacopeia (USP) for food supplements. Our operations follow the guidelines established by the Food and Drugs Administration (FDA), the Department of Agriculture and the United States Pharmacopoeia (USP). The Food and Drug Administration (FDA) inspects manufacturing processes about once a year.

The Quality Control Department has competent technical personnel that verifies and controls the quality of the entire production process, including the arrival of the raw materials, the manufacturing process and the finished products, performing the required physic-chemical analysis, supervising the packaging, labeling and storage of our products. The Quality Control process is overseen by a team of 12 professionals, which is integrated by pharmacist, analysts and chemical engineers with more than a decade of experience.

We maintain a vigilant focus on quality control, with a dedicated department overseeing all aspects of quality assurance. Our wellequipped laboratory conducts both chemical and microbiological tests on raw materials and final products. This rigorous approach ensures that we consistently meet the standards set forth by the FDA and the United States Pharmacopeia (USP)