I will provide ce marking, ukca, fda and gpsr compliance documents for amazon
ISO Compliance Consultant, ISO 27001, 9001 QMS, ISMS, Cybersecurity Specialist
About this Gig
Amazon asked for your CE, UKCA or GPSR documents? Listing blocked or suppressed? I prepare the compliance documentation you need to sell in the EU, UK and US.
What I provide:
- CE marking technical file and EU Declaration of Conformity
- UKCA technical file and UK Declaration of Conformity
- GPSR compliance pack: risk assessment, safety warnings, label and traceability content
- Standards mapping: LVD, EMC, RED, RoHS, Toy Safety, Machinery
- FDA establishment registration and device listing support
- Medical device CE (EU MDR) and FDA 510(k) document preparation
Why work with me:
- Clear scoping before you order, so no surprises
- Documents ready to upload to Amazon, eBay, Walmart and Etsy
- Editable Word and PDF files
- Fast replies and revisions included
Please note: I prepare the documentation. Lab testing, notified body certificates and FDA decisions are outside this gig.
Message me your product, target markets and photos for a free compliance check before ordering.
Language:
English
Platform:
E-Commerce stores
Delivery style preference
Please inform the freelancer of any preferences or concerns regarding the use of AI tools in the completion and/or delivery of your order.
FAQ
Can you help if Amazon blocked or suppressed my listing?
Yes. Send me a screenshot of Amazon’s notice. I’ll tell you exactly which documents it is asking for and prepare them for upload.
Do I need lab test reports?
For electronics, usually yes (EMC, LVD or RED). Send what you have and I’ll check whether it’s enough or what’s missing. Many simple products don’t need lab tests.
What is GPSR and do I need it?
GPSR is the EU General Product Safety Regulation. It applies to almost every non-food consumer product sold in the EU, including on Amazon EU.
. Can you register my company with the FDA?
I’ll guide you through establishment registration and device listing and prepare the information. You submit it through your own FDA account and pay the FDA fee.
Do you work on medical devices?
Yes, including EU MDR technical files, risk management (ISO 14971), clinical evaluation and FDA 510(k) documents. Message me first for a custom quote.
What files will I receive?
Editable Word files and ready-to-upload PDFs.
