I will do fda cosmetics registration and mocra compliance


About this gig
Are you in need of an FDA cosmetic registration, MoCRA compliance, cosmetic product listing, responsible person data or label review? I help beauty brands, manufacturers, importers, and private-label sellers organize the information needed for a practical U.S. compliance workflow.
I can review facility details, responsible person information, product names, ingredients, labels, US agent data, and renewal dates, identify missing information, prepare a structured submission checklist and create a product/facility tracker.
Premium buyers receive a launch pack covering safety record organization, adverse event workflow, renewal planning, and multi-product version control. This service supports preparation and documentation, it does not issue an FDA certificate, guarantee listing, certify product safety, or provide legal advice.
Send your product type, manufacturing role, facility country, label, ingredient list, and target US launch date before ordering so I can confirm the correct package.
Get to know Brandon Fasasi
Clear FDA filings and compliance for confident market entry
- FromUnited States
- Member sinceSep 2026
- Avg. response time1 hour
Languages
English
FAQ
Can you help register a cosmetic facility under MoCRA?
Yes. I can organize the facility information, registration fields, contact details, and renewal checklist. The responsible business must review and authorize the final submission.
Can you list multiple cosmetic products?
Yes. Standard and Premium packages can cover multiple products when the product count is agreed in advance. Each product needs accurate name, ingredient, label, and responsible person data.
Do you provide an FDA cosmetic certificate?
No. FDA states that it does not issue certificates or verification documents for cosmetic facility registration or product listing. I provide organized records and submission support instead.
Can you determine whether my small business is exempt?
I can perform a preliminary exemption screening review using the facts you provide. Certain product types are not covered by small business exemptions, so complex cases may need regulatory counsel.
Do you review cosmetic labels for MoCRA issues?
Yes. I can check whether key product and responsible person information appears consistent and flag obvious missing or conflicting details. This is not a formal legal label opinion.
Can you prepare an adverse event procedure?
Premium scope includes a practical workflow checklist for intake, escalation, records, and response ownership. It is not a substitute for a company’s validated safety or legal program.
Do you handle facility renewal reminders?
Yes. I can create a renewal calendar and tracker based on the initial registration date and your internal contacts. You remain responsible for monitoring deadlines and submitting updates.
Can you act as my US agent?
I can coordinate the information needed for a US agent and help compare the data requirements. Acting as an official agent requires a separate arrangement and is not automatically included.
Can you register products that make drug claims?
I can flag claims that may create a product classification concern. Products making drug claims may need a different regulatory pathway, so I will not promise cosmetic treatment for a drug product.
What information do you need for a cosmetic listing?
Send the facility details, responsible-person name, product names, ingredients, labels, manufacturing role, US agent details if relevant, and target launch date. I will confirm whether the scope is suitable.

