Tell us what is stalled, at risk, or consuming staff time.

No. AssayIQ can coordinate the technical workstream, structure questions and evidence, analyze agreed studies, and keep issues moving while the vendor and authorized laboratory leadership retain their responsibilities.

Within an agreed scope, AssayIQ can support the study plan, required validation or verification work, quality control setup, interference studies, documentation, issue tracking, training needs, and final handoff. Authorized laboratory leaders retain final approval.

No. Do not submit protected health information (PHI) or patient identifiers through the website or ordinary email. Any engagement requiring PHI begins only after roles, safeguards, transfer methods, and any required Business Associate Agreement are documented.

Small defined reviews begin with fixed launch pricing. Complex validations, implementation work, recurring support, and multi-site programs are quoted from the agreed scope, data readiness, turnaround, and deliverables.

No. AssayIQ develops transparent opportunity estimates and implementation options using agreed data and assumptions. Client finance, procurement, operational, quality, and clinical leaders validate the model and approve any action. Realized results depend on implementation and are not guaranteed.

The client does. AssayIQ provides consulting, analysis, documentation, and implementation support; authorized client leadership retains technical, clinical, regulatory, and operational approval.

Describe the delay, recurring problem, inspection concern, or decision your team cannot close. AssayIQ can convert that into a scoped discovery conversation without forcing you to diagnose the solution first.