Wei Laboratories Quality Standards
Our high quality, natural, herbal products are manufactured in our FDA licensed, CGMP compliant manufacturing facility located in Santa Clara, California. We embed the strictest quality and consistency standards in our manufacturing process. This allows us to attach our name to the product with pride.
Current Good Manufacturing Practices (CGMP’s) are regulations for the manufacture and sale of food, supplements, and pharmaceutical products, enforced by the US Food and Drug Administration (FDA).
Wei is subject to the Supplement CGMP standards for nutritional and herbal supplements (21 CFR Part 111).
- Packaging: The herbal supplement must be packaged and labeled as specified in the master manufacturing record. Ingredients: The manufacturers of all dietary ingredients used in the finished dietary supplements are required to follow CGMP standards for foods (21 CFR Part 117).
- Quality: The regulations for dietary supplements require manufacturers ensure the identity, purity, quality, strength and composition of both their ingredients and their finished dietary supplements.
- Hygienic Practices: The dietary supplement CGMP regulations include requirements for hygienic practices. This includes proper training of the personnel, cleaning of equipment, sanitation of the manufacturing plant, and in-process controls to ensure consistency of the product’s quality.
Our manufacturing process strictly follows CGMP standards to ensure that every finished product offers the same high efficacy and safety. Many aspects of our manufacturing practices far exceed the current FDA-enforced CGMP guidelines for dietary supplements.