R&D & Formulation Support

Accelerate development with data that de‑risks scale‑up and market claims.

• Analytical method development/validation; raw‑material qualification
• Stability and compatibility studies (accelerated/real‑time) with packaging interaction
• SPF/UVA, blue‑light, and antioxidant/anti‑pollution method guidance (as applicable)
• Instrumental performance testing (e.g., moisturization, TEWL, gloss, colorimetry)
• Sensory and consumer‑use studies with protocol design and statistical analysis

Microbiology & Preservative Efficacy

Safeguard product quality with robust microbial control programs.

• Total viable count, yeast/mold, and specified pathogen screening
• Preservative efficacy (challenge) testing aligned to recognized protocols
• Water quality monitoring and environmental controls for production sites

Toxicology & Safety Assessment

Build defensible safety files with expert toxicological review.

• Ingredient and finished‑product risk assessments; MoS/SED calculations where applicable
• Impurity and allergen profiling; residual solvent and heavy‑metal screening
• Safety documentation for market notifications and regulatory submissions

Regulatory & Market Access

Navigate evolving global rules with clear, practical guidance.

• Labeling, INCI listings, and claims alignment for destination markets
• Dossiers and notifications; PIF/CPSR support where applicable
• Post‑market surveillance, vigilance, and change‑control documentation

Manufacturing & GMP (ISO 22716)

Raise quality and reduce costs with fit‑for‑purpose systems and training.

• Gap analyses and implementation roadmaps for Cosmetics GMP
• SOP development, training, and eLearning tools; internal audits
• Contamination investigations and scale‑up troubleshooting with CAPA

Packaging & Supply Chain Assurance

Qualify materials and partners to secure quality at every hand‑off.

• Primary‑pack due diligence; extractables/leachables and compatibility checks
• Supplier audits and material specifications; CoA review and change control
• Distribution simulation and transport testing strategies (as applicable)

What You Can Expect

• Fast turnaround: many reports and certificates issued in 24–48 hours; expedited options available
• Transparent reporting: secure digital certificates, study reports, and regulatory documentation
• Standards‑first methods: ISO/IEC 17025, where applicable; recognized cosmetic protocols and GMP (ISO 22716)
• On‑site expertise: local teams at labs and production sites worldwide
• Strict chain of custody and data‑integrity controls from sampling through final reporting

Why Camin

• ISO/IEC 17025–accredited laboratories across 30+ countries
• Toxicologists, chemists, microbiologists, GMP and regulatory specialists
• Verified independence for impartial results and reduced dispute risk
• Operational efficiency that shortens time‑to‑market and lowers total cost

Who We Support

• Global manufacturers and international brands
• Retailers, importers, and private‑label owners
• Indie and contract manufacturers
• Packaging suppliers and raw‑material producers