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I need assistance with registering an already in-use disinfectant product under EU MDR for CE class IIA products. Key Requirements: - Verify and complete necessary technical documentation for CE certification. - Navigate the EU MDR regulatory landscape. - Ensure compliance with all safety and efficacy standards. Ideal Skills and Experience: - Experience with EU MDR and CE marking - Strong understanding of medical device regulations - Background in preparing technical documentation for certification
Project ID: 40374254
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7 freelancers are bidding on average $7,643 CAD for this job

Hi there, You need help getting your disinfectant product registered under EU MDR as a Class IIA device. I can help you navigate the process. Here is what I will do: - Review your current technical documentation - Identify gaps and complete missing sections - Ensure compliance with safety and efficacy standards - Guide you through the CE marking submission I have experience with EU MDR and medical device regulatory documentation. Send me your current product file and technical documents. Thanks, Revival
$5,000 CAD in 30 days
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Hello Already have something live to show you I am professional mobile software engineer with skills including Web Design, PHP, Website Development, Content Writing, Elementor, HTML, WordPress and Website Design. Please send a message to discuss more about this project. Always happy to hear from you Thanks
$7,500 CAD in 7 days
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Toronto, Canada
Member since Apr 15, 2026
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