Quality assurance
Quality, testing, and sourcing
Quality is the process; verification is the result on your specific batch. This page covers how Memory Vitali is made and tested before it reaches you.
Where it is manufactured
Memory Vitali is produced in the United States in a cGMP (current Good Manufacturing Practice) facility that operates in an FDA-registered environment. cGMP covers sanitation, equipment calibration, documentation, and traceability so that each run is consistent and accountable.
Independent third-party testing
Finished batches are tested by Linden Ridge Analytical, LLC, an ISO/IEC 17025 accredited laboratory that is independent of manufacturing. Testing every lot, rather than spot-checking, is how we keep label claims and bottle contents aligned.
What we test on every lot
- Identity and potency by HPLC, confirming the actives are present at expected levels.
- Heavy metals screening (lead, arsenic, cadmium, mercury) to < 0.5 ppm.
- Microbial screening for total counts and pathogens: Pass (USP <2021> / <2022> limits).
- Pesticide and contaminant checks against accepted thresholds.
- Allergen review: Non-GMO, gluten-free, with no soy or dairy in the formula.
From raw material to sealed bottle
Incoming ingredients arrive with supplier documentation and face identity and potency checks before production. Anything off-spec is rejected. After blending and encapsulation, the finished lot is tested again, assigned a batch code, and logged. Current run on record: MV26-RC-0418, certificate LR-COA-26-3307, with active purity of 99.2% via HPLC.