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ISO 17025 Accredited

Chemical Testing for FDA compliance

Reliable chemical testing designed for FDA compliance. ISO 17025 accredited methods with detailed reporting to meet your regulatory requirements.

ISO 17025 Accredited 48-Hour Turnaround Available 500+ Test Methods FDA-Compliant Reporting Dual Locations: Irvine & San Diego, CA

Quick Answer

Chemical Testing for FDA compliance ensures products meet the specific regulatory and quality standards required for market entry. ISO 17025 accredited laboratories like Qalitex provide validated testing methods, detailed COA reports, and expert guidance to support fda compliance processes efficiently.

Achieving fda compliance requires accurate, accredited laboratory testing that regulatory bodies and marketplace platforms trust. Qalitex Laboratories provides chemical testing tailored for fda compliance requirements. Qalitex Laboratories offers a full suite of chemical testing and analysis services for dietary supplement, food, and cosmetic brands. Our ISO 17025 accredited laboratory uses state-of-the-art instrumentation including HPLC, ICP-MS, GC-MS, LC-MS/MS, FTIR, and UV-Vis spectroscopy to deliver accurate, validated results. Our ISO 17025 accredited methods and detailed COA reports are designed to streamline your fda compliance process.

How Chemical Testing Supports FDA compliance

FDA compliance requires documented evidence of product safety and quality. Qalitex provides the specific testing and documentation needed to support your fda compliance process, including detailed COA reports, method validation documentation, and expert consultation on testing scope. Our ISO 17025 accreditation ensures your results are accepted by regulatory bodies and marketplace platforms.

Our Chemical Testing Capabilities

We cover the full range of chemical analysis needs: identity and authentication, potency and quantification, impurity profiling, contaminant screening (heavy metals, pesticides, solvents), and physical-chemical properties (pH, viscosity, moisture, water activity).

Method Development & Validation

For novel ingredients or products without pharmacopeial monographs, we develop and validate custom test methods per ICH Q2(R1). This includes selectivity, linearity, range, accuracy, precision, and robustness studies, producing a validated method suitable for regulatory submission.

Key Tests & Methods

Identity & authentication
Potency & quantification
Impurity profiling
Heavy metals (ICP-MS)
Pesticide residues (GC-MS/LC-MS)
Custom method development

Applicable Standards

ISO 17025 accreditationUSP, AOAC, ISO test methodsICH Q2(R1) method validationFDA cGMP 21 CFR Part 111

Industries We Serve

Dietary supplements
Food & beverage
Cosmetics & personal care
Raw material suppliers
Contract manufacturers

How It Works

Three simple steps to your results

01

Submit your samples

Ship samples to our Irvine or San Diego laboratory with your order form.

02

Testing & analysis

Our ISO 17025 accredited scientists run validated test methods.

03

Receive your CoA

Get a signed Certificate of Analysis within 48–72 hours.

FAQ

Frequently Asked Questions

What testing is required for fda compliance?

FDA compliance typically requires identity testing, purity analysis, potency verification, and contaminant screening. The exact panel depends on your product type and target market. Qalitex Labs can recommend the appropriate testing scope for your specific fda compliance needs.

How long does testing take for fda compliance?

Standard turnaround at Qalitex is 5–7 business days, with rush 48-hour service available for most test types. We recommend planning testing 2–3 weeks ahead of your fda compliance deadline to allow for any retesting if needed.

Is Qalitex Laboratories ISO 17025 accredited?

Yes. Qalitex Laboratories holds ISO/IEC 17025 accreditation, the international standard for testing and calibration laboratories. This ensures our methods, equipment, and quality systems meet the highest standards of accuracy and reliability.

What is your turnaround time?

Standard turnaround is 5–7 business days. Rush service with 48-hour turnaround is available for most test types. Contact us to discuss your timeline requirements.

What types of products do you test?

Qalitex tests dietary supplements (capsules, powders, gummies, liquids), cosmetics and personal care products, food and beverage items, botanical extracts, and raw materials. We serve brands, contract manufacturers, and Amazon FBA sellers.

How do I submit samples for testing?

Ship your samples to our Irvine or San Diego laboratory with a completed sample submission form. We provide prepaid shipping labels for qualifying orders. Results are delivered electronically via secure portal.

What chemical testing capabilities does Qalitex have?

Qalitex provides identity and authentication, potency and quantification, impurity profiling, contaminant screening for heavy metals and pesticides, residual solvent testing, and physical-chemical property testing using HPLC, ICP-MS, GC-MS, LC-MS/MS, FTIR, and UV-Vis spectroscopy.

Ready to get started?

Request a quote for chemical testing analysis for FDA compliance. Our team responds within 24 hours.