tags

Safety Testing
Efficacy Evaluation
Interpretation on Matters Concerning Cosmetic Registration and Filing by China NMPA

At a Glance: On July 29, 2026, China’s NMPA released new measures optimizing cosmetic registration and filing to enhance efficiency and stimulate industry innovation. Key reforms include exempting market-sale proof for foreign first-launch products, reducing animal testing, shifting ingredient safety files to enterprise archiving, allowing shared safety data for similar formulas, simplifying cross-border site transfers, and expanding flexible efficacy evaluation methods.

Cosmetic Efficacy Testing: Why Claim Substantiation Matters in 2026

Cosmetic efficacy testing has become an essential step in developing compliant, evidence-based cosmetic products. Whether launching a new skincare product, validating sunscreen SPF claims, or supporting anti-ageing marketing claims, brands increasingly need scientific evidence to demonstrate that their products deliver the benefits promised on the label. Consumers today expect greater transparency from cosmetic brands, while regulators worldwide are placing increasing emphasis on ensuring that cosmetic claims are truthful, substantiated, and supported by appropriate evidence. As a result, cosmetic efficacy testing plays a critical role in product development, regulatory compliance, and successful market access.

China Cosmetic Testing Requirements: CMA, CNAS, and ISO 17025 Explained

Not all cosmetic test reports are created equal: some are rejected by regulators, and some aren’t internationally recognized. Choosing the wrong laboratory can delay your product launch or even block market entry entirely. This article explains the differences between CMA, CNAS, and ISO 17025 accreditation, why they matter for cosmetic testing in China, and how to select the right lab for regulatory compliance.