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Claim validation studies that satisfy retail and regulatory scrutiny

ALS specializes in clinical testing for high-impact categories like anti-aging and skin renewal, helping meet consumer expectations while reducing regulatory risk. We align study design to support market claims such as "reduces appearance of fine lines" or "improves skin texture," delivering ready-to-use reports for leading retailers (Sephora, Ulta, Amazon, QVC, HSN) and global regulators.

ALS’ Clinical workflows prioritize:

  • Upfront feasibility assessments to reduce relabeling and launch delays.
  • ISO-aligned testing workflows with IRB reviews and clinically trusted, non-invasive methods.
  • Submission-ready reports designed to streamline regulatory and retail approvals.
  • Diverse test panels to ensure claims resonate across global audiences.

Whether you're finalizing a hero SKU or updating a core line, ALS helps ensure your claims are ready for market—without delay or ambiguity.

 

What you receive from clinical testing for anti-aging and skin renewal claims

  • IRB-reviewed clinical study reports with time-based efficacy endpoints
  • Quantitative and image-supported data on:
    • Visible wrinkle reduction (PRIMOS 3D, VISIA-CR, profilometry)
    • Elasticity and firmness (Cutometer, Quantificare 3D, Dermascan)
    • Texture and pore refinement (VISIA-CR, skin replica imaging)
    • Skin microstructure or density changes (confocal microscopy)
  • Typical panel sizes of 30-50 subjects, with timepoint options at baseline, week 2, week 4, week 8, and week 12
  • Statistical analysis of improvements using quantitative skin analysis tools
  • Submission-ready reports formatted for marketing, regulatory filing, and investor presentations.
  • Optional visuals, including time-lapse graphs and 3D renderings, to support consumer-facing marketing campaigns.
visia machine

Find out which claims are feasible for your product format

Why choose ALS?

  • Expertise you can trust: We focus on high-stakes clinical testing categories like anti-aging, delivering outputs trusted by global retailers and regulators.
  • Submission-ready results: Our reports are formatted for retail, marketing, and regulatory use, minimizing editing cycles and delays.
  • Market-relevant data: We recruit diverse subject panels to ensure claims are broadly defensible and impactful in the marketplace.
  • Proven methods: With ISO-aligned workflows and leading skin analysis tools, we deliver reliable results for wrinkle, firmness, and radiance claims.

How It Works

Process for clinical testing for anti-aging and skin renewal claims

  • Intake – Submit your formula, target claims, and launch goals. We’ll confirm feasibility and align you with the right clinical protocol.
  • Execution – We conduct studies using validated methods and diverse subject panels over defined time intervals.
  • Data – We capture wrinkle reduction, firmness, hydration, and radiance metrics using tools like PRIMOS 3D, Corneometer, and Chromameter.
  • Reporting – You receive submission-ready outputs tailored for regional regulators, retailer QA, and marketing claims support.

 

 

Global acceptance

Reliable Claim Support for Retailers and Regulators

  • IRB-reviewed clinical studies to substantiate claims like “reduces appearance of wrinkles,” “firmer skin,” and “improves texture”
  • Accepted by Amazon, Sephora, Ulta, QVC, HSN and specialty retailer QA teams
  • Standardized, non-invasive instrumentation across studies—PRIMOS (wrinkle depth), Cutometer (elasticity), VISIA-CR (pores and texture)
  • Timelines designed to align with formulation finalization and retail launch milestones
  • Submission-ready data formats for marketing, QA, regulatory, and investor use

 

Frequently asked questions

  • Does my product require testing to validate anti-aging claims?

    • Yes. Products making anti-aging or renewal claims, such as improving skin firmness, reducing appearance of wrinkles, or enhancing texture, typically require clinical substantiation to meet legal and regulatory standards.

      In the EU: Testing is required to comply with the Cosmetic Claims Common Criteria (Regulation (EU) No 655/2013) and the Technical Document on Cosmetic Claims. Results must be included in the Product Information File (PIF) under EU Regulation 1223/2009 to demonstrate compliance.

      In the U.S.: While MoCRA (Modernization of Cosmetics Regulation Act) enforces product safety substantiation, marketing claims are regulated by the FTC (Federal Trade Commission), which requires that all claims be truthful and supported by evidence.

  • What’s the difference between MoCRA and FTC requirements for U.S. products?

    • MoCRA (Modernization of Cosmetics Regulation Act): Focuses on product safety enforcement and requires proper product registration to ensure consumer safety.

      FTC (Federal Trade Commission): Oversees advertising claims, ensuring any marketing statements (e.g., “reduces wrinkles in 30 days”) are backed by reliable, scientific evidence.

  • Will claim validation testing delay my product launch?

     

    • Not necessarily. Claim validation testing timelines depend on product requirements and study designs. Interim results are often available during clinical studies to help prepare for launch or marketing timelines.

     

  • Can your testing reports be used for EU submissions?
    • Yes. Testing results that comply with the Cosmetic Claims Common Criteria (Regulation (EU) No 655/2013) are widely accepted. These testing endpoints are fully compatible with inclusions required under EU Regulation 1223/2009 in the Product Information File (PIF).