How is Activated Liquid Zeolite manufactured?
A. The manufacturing facility itself is certified to be cGMP-compliant (current-Good Manufacturing Practices) by the FDA. GMP is an FDA (Food & Drug Administration) term for the Quality Control and Quality Assurance (QA/QC) procedures that are standard in the facility. This also includes training of the personnel, storage of materials and micro-analysis of the product. The manufacturing process takes approximately five to seven days. Some of the finished product is sent for analysis using Thin-Layer Chromatography (TLC) and High-Performance Liquid Chromatography (HPLC). The product is also sent through a detailed micro-analysis, where it is evaluated for any sort of contamination (bacterial, moulds, spores, etc.). Finally, some bottles from every batch are retained so that these can be tested on a future date if it becomes necessary. We also periodically inspect the manufacturing facility and all of their batch records.
