Analytical Chemistry
Identity, potency, impurities, heavy metals, and residual solvents across five specialized chemistry groups — HPLC, LCMS, GC/GCMS, IC/ICPMS, and Wet Chemistry.
ISO 17025 Accredited · Dallas, TX
BioChroma is a full-service analytical and microbiology testing laboratory supporting product release, stability programs, and regulatory compliance for pharmaceutical and consumer product programs.
Operational view
Identity, potency, impurities, heavy metals, and residual solvents across five specialized chemistry groups — HPLC, LCMS, GC/GCMS, IC/ICPMS, and Wet Chemistry.
Microbial limits (USP <61>/<62>), preservative efficacy (USP <51>), endotoxin (USP <85>), sterility, pathogen screening, environmental monitoring, and species identification.
ICH-compliant stability studies including accelerated, long-term, photostability, and forced degradation — with protocol design and trend reporting.
PCR, RT-PCR, Next-Generation Sequencing, species identification, authentication, and adulteration detection.
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.
Testing disciplines
Identity, potency, impurities, heavy metals, and residual solvents across five specialized chemistry groups — HPLC, LCMS, GC/GCMS, IC/ICPMS, and Wet Chemistry.
Explore Analytical ChemistryMicrobial limits (USP <61>/<62>), preservative efficacy (USP <51>), endotoxin (USP <85>), sterility, pathogen screening, environmental monitoring, and species identification.
Explore MicrobiologyICH-compliant stability studies including accelerated, long-term, photostability, and forced degradation — with protocol design and trend reporting.
Explore Stability ProgramsPCR, RT-PCR, Next-Generation Sequencing, species identification, authentication, and adulteration detection.
Explore Molecular BiologyFormulation support, R&D testing, in vitro bioavailability, consulting, and launch readiness for products moving toward market.
Explore Product DevelopmentDownload the sample submission form and coordinate logistics for incoming samples.
Download Submission FormBuilt for defensible results
Testing follows documented methods under controlled, auditable conditions. Our accreditation provides third-party verification of technical competence.
USP, AOAC, FDA BAM, EP, and ICH methods executed by trained analysts across chemistry, microbiology, and stability disciplines.
Every dataset undergoes independent QC review. Our data integrity practices are designed to produce results that are attributable, legible, contemporaneous, original, and accurate.
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
How we work
Define what needs to be tested, methods, and deliverables.
Samples are processed across the relevant analytical disciplines.
Results are reviewed, verified, and delivered in usable formats.
Data supports your release, filing, or quality decisions.
Get started
Email sales for project scoping, timelines, and quotes.
Reach chemistry, microbiology, product development, quality, or operations directly.
Download the submission form for incoming sample logistics.
Call the lab during business hours.
Next step
Tell us your product, your timeline, and what decision the testing needs to support. We will connect you to the right department.