PFAS (Per- and Polyfluoroalkyl Substances) are a large group of fluorinated substances with widespread industrial and consumer product applications, characterized by strong carbon-fluorine bonds that make them resistant to degradation.

How do I determine whether my product complies with PFAS requirements?

Compliance evaluation depends on jurisdiction, substance identity, product type, intended use, concentration, and the specific regulatory requirements in effect. SciQra evaluates these factors to identify applicable obligations and compliance gaps.

How do I request PFAS safety and regulatory support from SciQra?

You can request PFAS safety and regulatory support by contacting SciQra at info@sciqra.com or +1-609-917-6181, or through the contact form at sciqra.com/contact-us. Scope and timeline depend on the product type, ingredients involved, and target markets.

PFAS Safety And Regulatory Support

Q: Why are PFAS considered a concern?

Certain PFAS substances have been associated with persistence, bioaccumulation, environmental distribution, and potential human health effects, which is why they are increasingly subject to regulatory scrutiny and reporting requirements.

Q: Are PFAS regulated in cosmetics?

Yes, PFAS regulation in cosmetics depends on the specific substance, jurisdiction, product type, and intended use, with requirements varying across markets such as the United States and the European Union.

PFAS Safety And Regulatory Support

With our PFAS experts, we support organizations in addressing the scientific, toxicological, human health risk, and regulatory considerations associated with Per- and Polyfluoroalkyl Substances (PFAS) across ingredients, raw materials, formulations, and products for diverse industries, including cosmetics, consumer care, and specialty chemicals.

Our Support Includes:

PFAS Regulatory & Compliance Support

Evaluation of PFAS regulatory applicability based on intended market
Identification of ingredients, raw materials, formulations, products, and components potentially impacted by PFAS requirements
Assessment of applicable PFAS restrictions, prohibitions, thresholds, and reporting obligations
Identification of compliance gaps and potential business impacts
Review and preparation of supporting information or documents required for regulatory compliance and submission
PFAS reporting under Toxic Substances Control Act (TSCA) Section 8(a)(7)
Scientific review of PFAS-related claims, including “PFAS-Free” and “No Intentionally Added PFAS”

PFAS Toxicological Risk Assessment

Preparation of Toxicological Risk Assessment report and scientific summaries of PFAS, related substances, and potential alternatives
Compilation and review of available scientific and toxicological information
Assessment of relevant toxicological endpoints, including available epidemiological and human health evidence
Review of toxicokinetic, persistence, and bioaccumulation information
Evaluation of potential risks associated with products, including exposure assessments and hazard identification
Identification of data gaps associated with PFAS, related substances, and alternative ingredients
Evaluation of the need for additional analytical, exposure, or toxicological data
Review and interpretation of available analytical data
Identification of information required to support safety, risk, and regulatory assessments

Frequently Asked Questions

What are PFAS?

PFAS (Per- and Polyfluoroalkyl Substances) are a large group of fluorinated substances with widespread industrial and commercial applications. Many PFAS are characterized by strong carbon–fluorine bonds and, depending on the substance, may exhibit high environmental persistence.

Why are PFAS considered a concern?

PFAS are receiving increasing scientific and regulatory attention because certain substances have been associated with persistence, bioaccumulation, environmental distribution, and potential human health effects.

What is a PFAS risk assessment?

A PFAS risk assessment integrates information on the potential hazards of a PFAS substance with relevant exposure information to characterize potential human health risks. The assessment may include toxicology, exposure assessment, dose–response information, and uncertainty evaluation.

Are PFAS regulated in cosmetics?

PFAS can be subject to restrictions or other regulatory requirements in cosmetic products depending on the substance, jurisdiction, product type, and intended use. Cosmetic companies should evaluate PFAS requirements for each relevant market rather than assuming that one global requirement applies to all products.

How to determine whether product is compliant with PFAS requirements?

Compliance depends on the applicable jurisdiction and the specific substance, product, use, concentration, and regulatory requirements. SciQra can evaluate these factors, identify applicable restrictions or thresholds, and highlight potential compliance gaps.