MoCRA Compliance & Cosmetic Regulatory Solutions

LexisNexis Life Sciences SolutionsCosmetics Solutions
End-to-end SPL product listing submissions, ensuring accurate, compliant data for MoCRA requirements.

What are LexisNexis cosmetic regulatory compliance and MoCRA solutions

LexisNexis Life Sciences Solutions cosmetic services navigate SPL requirements by managing structured product labeling submissions end to end, ensuring compliance with MoCRA requirements. Leveraging a proven XML data standard used across regulatory programs, we deliver accurate, consistent, and submission-ready data.

Cosmetic Product Listing & Facility Registration
gulatory Submissions & eCTD Complexity

FDA SubmissionsStreamline cosmetic product listing and facility registration

MoCRA requires cosmetic companies to submit product listings and facility registrations to the FDA. LexisNexis Life Science Solutions helps organizations collect required product and facility data, populate regulatory forms, and prepare Structured Product Labeling submissions for accurate and efficient regulatory filing.

Cosmetic Safety Documentation & GMP Compliance

Product SafetyMaintain compliant manufacturing and safety documentation

Cosmetic companies must maintain safety substantiation records demonstrating that products are safe for intended use. Our regulatory experts help organizations manage ingredient safety documentation, product testing records, and compliance documentation needed to meet FDA requirements and support regulatory inspections.

MoCRA Compliance Services for Cosmetics

MoCRA CompliancePrepare for MoCRA compliance with expert guidance

LexisNexis Life Sciences Solutions provides MoCRA awareness training and regulatory consulting designed to help cosmetic companies understand new regulatory obligations. Our experts explain the responsibilities of the “responsible person,” key compliance deadlines, and the operational steps organizations must take to meet regulatory expectations while minimizing risk.

Cosmetic Regulatory Compliance Services & Solutions


Cosmetics regulatory services supporting MoCRA compliance

Cosmetic form population

Support identifying required regulatory information and populating FDA forms accurately and efficiently.

Regulatory readiness assessment

A structured evaluation that helps organizations identify regulatory gaps and prepare for upcoming compliance deadlines.

Product data & facility listing

Preparation and submission of cosmetic product listings and facility registrations to the FDA using structured submission formats.

Data Security, Privacy, and Governance

Security and privacy you can count on

Privacy by design

LexisNexis protects customer data wherever it is stored, sent, or accessed. We apply privacy by design principles at every stage of development to ensure security and compliance are built in from the start. Our advanced encryption and rigorous compliance protect your sensitive information. 

Strict security protocols

LexisNexis systems meet the highest standards for information security. We partner with trusted, enterprise-grade cloud providers, continuously monitor and improve our infrastructure,

MoCRA Compliance & Cosmetic Regulatory Solutions FAQs

Frequently asked questions

Cosmetic regulations vary by market. In the U.S., this includes MoCRA requirements such as facility registration and product listing, while in the EU it involves CPNP notifications and ingredient compliance. We help you navigate global requirements to ensure your products meet all applicable regulations.

Structured Product Labeling (SPL) is an XML-based format used by the FDA for product submissions. Under MoCRA, SPL is used for cosmetic product listings and facility registrations. We manage the creation, validation, and submission of SPL files to ensure compliance.

Yes. Under MoCRA, manufacturers and processors must register their facilities and list their cosmetic products with the FDA. Our team helps ensure accurate, timely submissions and ongoing compliance.

Cosmetic labeling must meet specific requirements for ingredients, claims, and formatting depending on the market. We provide guidance and validation to help reduce risk and avoid compliance issues.

We provide end-to-end support—from regulatory guidance and data structuring to SPL submission and ongoing updates—helping you streamline compliance and bring products to market with confidence.

Our expanded Regulatory Advisory Team can assist you with a wide variety of tasks and topics. Click on the Inquire Now button above or Choose Plan and fill out a few brief comments about your needs in order to facilitate an appointment. We look forward to learning more about how we can assist you.
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Reed Tech is now LexisNexis Life Sciences Solutions

While the Reed Tech name is being retired, the business has long operated as part of LexisNexis. Customers will continue to work with the same regulatory experts, services, and solutions—now unified within LexisNexis Life Sciences to reflect the broader capabilities and global resources of LexisNexis