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Whether you're preparing for URAC/ACHC accreditation, fulfilling annual PQ requirements, or securing payor compliance, QualQ™ takes cold chain testing off your plate and puts it into expert hands.
Compliance Made Easy
Our all-in-one cold chain PQ testing service takes your existing cold chain or CRT pack-outs and validates them under real-world conditions. You stay focused on patients while we deliver the proof.
Lightning-Fast Turnaround
From box-in-hand to draft report in just 72 hours.
Expert Support From Start to Finish
You get a free 15-minute consulting call and access to our decade of cold chain PQ experience.
QualQ™ simplifies the thermal validation process for CRT and refrigerated medications, saving your internal team time while ensuring you’re inspection-ready with audit-proof documentation.
QualQ™ helps protect the integrity of blood products during storage and transport, aligning with AABB cold chain standards. With over a decade of experience, MaxQ’s scientific approach gives your team confidence in compliance, patient safety, and operational performance.
Deliverables designed to pass inspections with confidence, including:
Detailed analysis of every temperature excursion during PQ testing — duration, magnitude, and root-cause assessment with corrective recommendations. Reviewed against your acceptance criteria.
Executive summary letter formatted for URAC, ACHC, and AABB auditor review. Cites validation methodology, test conditions, and pass/fail outcomes against your specifications.
Photographic evidence of pack-out arrival condition for every test cycle — documenting the integrity of seals, ice, and payload position. Inspection-ready imagery your auditor wants to see.
Every temperature logger used in your validation is NIST-traceable, calibrated within tolerance, and documented with calibration certificates included in the report package.
Full temperature/time profile graphs for every validation cycle — payload, ambient, and probe locations charted with min/max excursion bands. Audit-ready chart deliverables.
We partnered with MaxQ to validate our cold chain packaging across seasonal extremes, ensuring our processes perform reliably under real-world conditions. Through continuous monitoring and analysis of environmental data across our supply chain, MaxQ has enabled us to consistently protect the integrity of our temperature-sensitive pharmaceutical products, from manufacturer to patient. We look forward to continuing our collaboration with MaxQ, driven by their commitment to scientific rigor and data accuracy. This collaboration has been crucial in providing us with an additional means of safeguarding the patients who rely on our medications.
Get cold chain validation done right. Send us your pack-out, your shipping
profile,and your compliance window. We'll deliver an audit-ready PQ report
in 72 hours. Schedule a free 15-minute consult or request a quote.
Efficient Solutions, Exceptional Results.