Private briefing · By invitation
Assay-A is the trade name of Assay-A Healthtech Software Services LLC (US registration pending), an independent standards authority supporting formulation review, accountable batch records and paired-code traceability for manufacturers and regulatory partners worldwide.
The problem
Honest manufacturers see their products copied. Patients cannot tell real from fake. Regulators are fighting alone. Assay-A gives all three the same source of truth.
Every recipe is screened for excipient interactions, pharmacopeial limits and tropical Zone IVb stability before it reaches a line.
An independent Assay-A pharmacologist reviews and stamps the formula. Once approved, its fingerprint is frozen — it cannot be quietly changed.
Each production lot receives a fixed number of paired codes — one for the box, one for the container inside. No more, no less.
Anyone scans with an ordinary phone camera. No app, no SMS, no scratch card. A repeated inner-code scan raises an investigation signal.
Two codes, one truth
Outer codes support shelf checks. Repeated inner-code scans and pairing mismatches raise review signals. A legitimate rescan can also trigger an alert; laboratory evidence and human investigation remain essential.
Step 1 · Outer box

Code on the carton
Checks the registered lot, manufacturer and expiry without using the inner code.
Step 2 · Inner container

Code on the container
Paired with its carton. Repeat scans and mismatches raise investigation signals.
Illustrative packaging · not live verification codes
Who works on Assay-A
Prove your products are yours. Protect your brand from counterfeiters and reach market faster with sealed dossiers.
Read-only oversight of certified formulas, batch registers and a live map of where copied codes are surfacing.
Our independent reviewers hold the stamp. Manufacturers can never approve their own formulas.

Assay-A does not manufacture medicines and holds no stake in any product it certifies. Our tools support — and never replace — laboratory testing and national regulatory approval.