Scivation

The Scivation scientific affairs team is not only architecting research and ingredient substantiation, but they are constantly compiling structure function documentation and ingredient dossiers. QA/QC departments are engaged in external and internal FDA-compliant audits for Good Manufacturing Practices (GMPs), including documenting proper standard operating procedures (SOPs) and to ensure that proper use (and interpretation) of analytical testing methods and equipment. These and other behind-the-scenes compliance measures provide the constant cadence — the scientific drumbeat — to which Scivation orchestrates its product innovation and development.
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