ISO 17025 Accredited · Dallas, TX

Your product is ready. Your testing data should be too.

BioChroma is a full-service analytical and microbiology testing laboratory supporting product release, stability programs, and regulatory compliance for pharmaceutical and consumer product programs.

  • Dallas laboratory founded in 2014
  • Compendial chemistry, microbiology, and stability support
  • Direct routing to technical teams and department leadership

Operational view

One lab. Multiple disciplines. Coordinated release decisions.

Analytical Chemistry

Identity, potency, impurities, heavy metals, and residual solvents across five specialized chemistry groups — HPLC, LCMS, GC/GCMS, IC/ICPMS, and Wet Chemistry.

Microbiology

Microbial limits (USP <61>/<62>), preservative efficacy (USP <51>), endotoxin (USP <85>), sterility, pathogen screening, environmental monitoring, and species identification.

Stability Programs

ICH-compliant stability studies including accelerated, long-term, photostability, and forced degradation — with protocol design and trend reporting.

Molecular Biology & PCR

PCR, RT-PCR, Next-Generation Sequencing, species identification, authentication, and adulteration detection.

0 Years Operating
0 Analytical Groups
0 Scientists & Staff
ISO 17025 Accredited

Operational depth

Founded in 2014, BioChroma operates six analytical groups and a dedicated microbiology department from our Dallas laboratory — supporting product release, shelf-life decisions, and regulatory review across OTC, pharmaceutical, dietary supplement, and consumer product programs.

Built for defensible results

Accredited systems, compendial methods, and documented quality practices designed to withstand regulatory scrutiny.

ISO 17025 accredited laboratory

Testing follows documented methods under controlled, auditable conditions. Our accreditation provides third-party verification of technical competence.

Compendial method expertise

USP, AOAC, FDA BAM, EP, and ICH methods executed by trained analysts across chemistry, microbiology, and stability disciplines.

ALCOA+ data integrity

Every dataset undergoes independent QC review. Our data integrity practices are designed to produce results that are attributable, legible, contemporaneous, original, and accurate.

Direct scientist access

Your project is managed by department directors and group leads who can answer technical questions directly — no ticket queues between you and the people doing the work.

Products we test

Finished goods and manufactured products across regulated and consumer categories.

Pharmaceutical

OTC drug productsPrescription pharmaceuticalsTopical and transdermal productsOral and liquid formulations

Consumer

Cosmetics and personal careHousehold and consumer care

Food & Supplements

Dietary supplementsFood and beveragesBotanicals

How we work

From scope to release — a clear path through testing.

01

Scope

Define what needs to be tested, methods, and deliverables.

02

Test

Samples are processed across the relevant analytical disciplines.

03

Report

Results are reviewed, verified, and delivered in usable formats.

04

Release

Data supports your release, filing, or quality decisions.

Next step

Not sure where to start?

Tell us your product, your timeline, and what decision the testing needs to support. We will connect you to the right department.