One regulated-equipment program for the bench, the cleanroom, and the cold storage

What we deliver to biotech operators

• Bench instrument calibration — pipettes, balances, thermometers, dataloggers, pH meters, spectrophotometers, centrifuges, mixers, shakers, environmental monitors, dataloggers. A2LA Cert 2039.01.
• Pipette & liquid handler calibration — single-channel, multi-channel, electronic, and bench-mounted handler programs. ISO 8655 gravimetric method.
• Lab centrifuges, mixers, shakers, incubators — RPM, RCF (g-force), temperature, time. Onsite or in our Webster lab.
• ULT freezer, biorepository, and stability chamber mapping — IQ/OQ/PQ qualification reports with mean kinetic temperature (MKT) calculation. The mapping deliverable cell & gene therapy auditors actually open.
• Biosafety cabinet certification — NSF/ANSI 49 Class I, II (A1/A2/B1/B2/C1), Class III. NSF/ANSI 49 Field Certifier credentialed.
• Cleanroom certification — ISO Class 5/7/8 recertification for cGMP manufacturing suites, fill-finish rooms, and translational labs. CETA RCCP and NSF Accredited Technicians.
• Accredited environmental monitoring — viable air, surface, gloved fingertip, media fill. A2LA Cert 7533.01 incubation and microbial ID by Taylor Lake Laboratories.
• Cleanroom commissioning — Precision Biotech Solutions delivers IQ/OQ/PQ for new biotech manufacturing space. ISO 14644 classification, HEPA integrity, NEBB TAB.
• Fume hood certification — ANSI/ASSP Z9.5 ventilation verification for chemistry and BSL-2 spaces.
• Analytical / pH / spectrophotometry calibration — for the QC bench instruments biotech operators run alongside their main workflows.

Why biotech operators consolidate with Allometrics

One accreditation chain that scales with you. Most calibration vendors lose value as a biotech operator moves from research-only to clinical manufacturing — the small-shop vendor doesn't carry A2LA accreditation, the cGMP-only vendor doesn't want the bench work. Allometrics serves bench biotech with the same accreditation chain that supports cGMP manufacturing — so the program scales with your stage.

One Group across commissioning, recertification, calibration, viables, and mapping. When Precision Biotech Solutions commissions a new cleanroom, the data is on file with the same organization that performs the recurring recertification, calibrates the equipment, and analyzes the viables. Most biotechs split this across vendors who never share data; Allometrics keeps it in one place.

Houston life-sciences cluster fluency. Long-running relationships with major academic medical centers, NCI-designated cancer centers, medical schools, and specialty research institutes across the Texas Medical Center — including cGMP cores supporting drug development, cell therapy, viral vector, and RNA work. We know the inspectors, the QMS templates, and the IRB / IBC review cycles your biotech is moving through.

Audit-time guarantee. If a calibration, certification, or qualification report we delivered is challenged in an FDA, sponsor, IBC, or partner audit, we will address it. Records on IndySoft — 21 CFR Part 11–compliant electronic records.

50 years of regulated-environment experience. Founded 1976. 1,800+ customer accounts. A team that has seen biotech evolve from monoclonal antibodies to mRNA platforms.