HoneyPezil Manufacturing Standards: cGMP Compliance & Quality Control
Every bottle of HoneyPezil is compounded under strict federal standards in an audited, FDA-registered US facility adhering to 21 CFR Part 111 cGMP regulations.
Raw Material Identity Quarantine
All incoming raw botanical extracts and amino acids are placed in physical quarantine and tested via HPLC and FTIR spectroscopy against certified reference standards before release into production.
USP <2232> Heavy Metal Screening
Finished capsules are screened via Inductively Coupled Plasma Mass Spectrometry (ICP-MS) to confirm lead (<0.50 ppm), arsenic, cadmium, and mercury are well within strict safety limits.
USP <2021/2022> Bioburden Screen
Microbiological plating confirms total aerobic counts below 100 CFU/g and complete absence of pathogens including Salmonella and E. coli.
Automated Cleanroom Encapsulation
Compounded in positive-pressure cleanrooms with continuous HEPA filtration and relative humidity regulation below 45% to prevent amino acid clumping.