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I will prepare fda mocra cosmetic compliance documentation, procedures and records
ERROL AUSTEN
About this gig
Launching cosmetic products in the USA? I can help your business prepare professional FDA MoCRA compliance documentation to support regulatory requirements. I create customized quality documents, SOPs, procedures, records, and templates for cosmetic manufacturers, private label brands, importers, and distributors.
Services include: FDA MoCRA documentation, Cosmetic SOPs, Quality Procedures, Batch Manufacturing & Packaging Records, Product & Raw Material Specifications, Finished Product Specifications, Cleaning Procedures & Logs, Equipment Calibration Records, Complaint Handling, Serious Adverse Event Reporting, Change Control, CAPA, Document Control, Training Records, Supplier Qualification, Risk Assessments, Cosmetic GMP Documentation, Safety Documentation Templates, Internal Audit Documents, and Record Templates.
Why choose me? Customized, professional, editable Word documents, fast delivery, confidential service, and unlimited revisions with Premium. Please contact me before placing your order to discuss your requirements.
Get to know ERROL AUSTEN
ERROL AUSTEN
FDA Compliance and Regulatory Documentation Expert
- FromCanada
- Member sinceJul 2026
- Avg. response time15 hours
Languages
English, Spanish, French, German
I am a Quality Management System (QMS) documentation specialist helping medical device, pharmaceutical, and healthcare companies develop professional regulatory documents.
I create FDA-focused quality documentation including SOPs, Quality Manuals, CAPA procedures, complaint handling procedures, internal audit documents, and quality forms
My services focus on creating clear, organized, and audit-ready documentation aligned with industry quality practices and regulatory expectations.
I can support companies building a new QMS, improving existing documentation, or preparing for quality audits.
Other Regulatory Compliance Consulting Services I Offer
FAQ
What is MoCRA?
The Modernization of Cosmetics Regulation Act (MoCRA) establishes new FDA requirements for cosmetic companies, including facility registration, product listing, adverse event reporting, safety substantiation, and records requirements.
Do you provide FDA registration?
No. I prepare documentation that supports compliance. FDA facility registration and cosmetic product listing are submitted separately through FDA systems when applicable.
Is this documentation customized?
Yes. All documents are prepared according to your business activities and products.
