Quality & Testing

Quality & Testing

How we ensure every Pilly Labs product meets the highest standards for safety, purity, and potency.

Manufacturing Standards

All Pilly Labs products are manufactured in the United States in facilities that are:

  • FDA-registered — Our manufacturing facilities are registered with the U.S. Food and Drug Administration as required for dietary supplement production.
  • GMP-compliant — We follow Current Good Manufacturing Practices (cGMP) as defined by 21 CFR Part 111, the FDA regulation governing dietary supplement manufacturing.

These standards cover every stage of production — from raw material receiving and identity testing through manufacturing, packaging, labeling, and storage.

Our Quality Process

  1. Raw Material Verification — Incoming ingredients are tested for identity to confirm they match what's on the label.
  2. Contamination Screening — Materials are screened for common contaminants including heavy metals, microbial contamination, and other adulterants.
  3. Manufacturing Controls — Production follows documented standard operating procedures (SOPs) with in-process quality checks.
  4. Finished Product Testing — Final products undergo testing to verify potency, purity, and consistency before release.
  5. Label Accuracy — What's on the label is what's in the product. Full ingredient panels with exact dosages. No proprietary blends.

Ingredient Transparency

We believe transparency is non-negotiable. For every Pilly Labs product:

  • Every ingredient is listed on the label with its exact amount
  • We never use proprietary blends that hide individual ingredient dosages
  • We identify the source and form of each key ingredient (e.g., "Reishi Extract" vs. generic "mushroom blend")
  • Full ingredient information is available on every product page on our website

What We Avoid

  • Artificial colors and synthetic dyes
  • Proprietary or "secret" blends
  • Misleading dosage claims
  • Ingredients without published safety data

Regulatory Compliance

Pilly Labs complies with all applicable U.S. regulations for dietary supplement manufacturing and marketing, including:

  • DSHEA (Dietary Supplement Health and Education Act) — Our products are classified and marketed as dietary supplements in accordance with federal law.
  • FDA 21 CFR Part 111 — Our manufacturing facilities follow Current Good Manufacturing Practices for dietary supplements.
  • FTC Act — All marketing claims comply with Federal Trade Commission guidelines for truthful, non-deceptive advertising.
  • Supplement Facts labeling — Our labels follow FDA requirements for dietary supplement labeling under 21 CFR Part 101.

Questions About Our Quality

We welcome questions about our ingredients, sourcing, manufacturing, and testing. Please contact us at info@pillylabs.com or call (708) 697-9131.

*These statements have not been evaluated by the Food and Drug Administration. Our products are not intended to diagnose, treat, cure, or prevent any disease.