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Dietary Supplement Stability Testing Services

Prove your product's quality over time with FDA-compliant stability & shelf life testing.

Supplement stability testing evaluates how a dietary supplement performs under various environmental conditions — temperature, humidity, and light — over time, following ICH Q1A(R2) protocols to validate that products remain safe, potent, and effective throughout their claimed shelf life.

Qalitex Laboratories specializes in dietary supplement stability testing that ensures your products remain safe, potent, and effective throughout their intended shelf life. Our testing services comply with FDA regulations, follow GMP standards, and support your product's market longevity.

What Is Stability Testing and Why It Matters

Stability testing evaluates how a dietary supplement performs under various environmental conditions — temperature, humidity, and light. We conduct both real-time and accelerated stability studies per ICH Q1A(R2) guidelines, assessing active ingredient potency, microbiological integrity, packaging durability, and organoleptic properties (color, odor, texture).

Shelf Life Testing

Shelf life testing defines how long a supplement remains both safe and effective, providing the data needed for accurate expiration dating. We simulate extended storage under real and accelerated conditions, testing at 0, 1, 3, 6, and 12 months, evaluating degradation of actives and risk of microbial growth.

Our Testing Process

We test a wide range of formats: tablets, capsules, softgels, powders, gummies, and liquids. Every study includes a protocol design phase, appropriate chamber conditions (ICH Zone I–IV), testing intervals, and a final stability report with CoA documentation suitable for FDA submission.

Ensayos y métodos incluidos

  • Real-time stability studies
  • Accelerated stability (ICH Q1 conditions)
  • Potency & label claim over time
  • Microbial integrity testing
  • Packaging compatibility
  • Organoleptic evaluation

Normas y conformidad regulatoria

  • ICH Q1A(R2)
  • FDA Guidance for stability testing
  • USP dietary supplement standards
  • cGMP 21 CFR Part 111

Sectores que atendemos

  • Dietary supplements (all formats)
  • Nutraceuticals
  • Functional foods
  • Amazon FBA products requiring expiry dating
  • Contract manufacturers
ISO 17025

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📍 Irvine, CA · San Diego, CA
⏱ 2–12 weeks plazo de entrega
🌍 Clientes en todo el mundo

Preguntas frecuentes

What is the difference between real-time and accelerated stability testing?

Real-time stability testing stores products under normal conditions and tests at intervals over months or years, while accelerated stability testing uses elevated temperature and humidity to predict shelf life faster. Qalitex performs both types per ICH Q1A(R2) guidelines.

How long does a stability study take?

Accelerated stability studies typically run 3–6 months under ICH conditions (40°C/75% RH). Real-time studies run 12–36 months under normal storage conditions. Qalitex tests at 0, 1, 3, 6, and 12 months to track changes in potency, microbiology, and organoleptic properties.

Why do supplements need stability testing?

Stability testing validates that a dietary supplement remains safe, potent, and effective throughout its claimed shelf life. The FDA requires stability data to support expiration dating, and retailers like Amazon require documented shelf-life validation.

Por qué las marcas eligen Qalitex para supplement stability testing

⏱️

Entrega en 48 h

CoA firmado en 48–72 horas

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Acceso directo al científico

Hable con el químico que realiza sus ensayos

🤝

Sin pedido mínimo

1 SKU o 100 — la misma calidad

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Aviso legal: Los resultados de los ensayos proporcionados por Qalitex Laboratories son datos analíticos destinados a fines de control de calidad. No constituyen asesoramiento legal, regulatorio ni de conformidad. Los clientes son los únicos responsables de garantizar que sus productos cumplen todas las normativas federales, estatales y locales aplicables.