Enterprise QA
Enterprise Peptide & API Quality Assurance.
Three kinds of organizations carry the most exposure in this supply chain. Each gets the full Tekmeris Standard, scoped to its actual risk. Enterprise programmes span all seven annexes — supplier panels, facility networks, and device fleets under one contract.
Counterparty Risk
Your “Factory” Might Not Be a Factory.
A significant share of overseas “manufacturers” are trading companies, distributors, or the international sales office of a manufacturer located elsewhere. A warehouse is not a production line. A sales office cannot be blind-sampled. Before money moves, our Phase-0 vetting matches your contract counterparty against the business-license scope, the GMP certificate holder, and the state enterprise credit registry. If your counterparty is an intermediary, we trace through to the true manufacturer, or we tell you, in writing, that a production run cannot be verified with this counterparty.
TEKMERIS will never sell a warehouse inspection as a factory audit.
Functional medicine clinics
Protect your patients and your medical licence. Ensure every vial meets the highest purity standards before it enters your clinic, with independent documentation to prove it.
Supplement & peptide brands
Scale your brand without supply chain anxiety. We act as your outsourced Chief Quality Officer in Asia, vetting, auditing, and blind-testing so your name never rides on an unverified batch.
Private equity / healthcare roll-ups
Conduct pre-acquisition supply chain due diligence. We verify the physical reality of your target's overseas vendor relationships before the deal is priced.
Peptide Purity Testing: HPLC, IEX, ICP-MS & Endotoxin Panels.
Blind samples are routed to ISO 17025 laboratories for analytical HPLC purity and peak table, IEX-HPLC charge variants, MS/MS identity confirmation, ICP-MS heavy metals, residual solvents, net peptide content, and endotoxin panels for injectable-grade material.
Every enterprise engagement runs the full 3-Phase Verification Protocol (vetting, physical audit, blind verification) under one chain of custody and one report. Scope and pricing are set after a written review of your intake brief, so you pay for the verification your supply chain needs and nothing else.
Our audit protocol operates on a strict silence policy. To preserve forensic integrity, we do not release interim findings, locations, or operational logistics during the field audit. The only communication of results is the final, cryptographically sealed Verification Dossier.
Responsibilities at a Glance
TEKMERIS verifies batch integrity and factory provenance at the point of origin. The Client remains the sole Importer of Record. Customs clearance, import permits (FDA/TGA/MHRA), and border seizure liability are the sole responsibility of the Client.