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I will do mhra registration, ukca certification, medical device compliance and mdr docu
Viva Lucas
About this gig
Are you looking to sell your medical device in the UK but struggling with MHRA registration or UKCA compliance?
I will help you complete your MHRA registration, UKCA certification, and medical device compliance so your product can be legally placed on the UK market.
I specialize in MHRA medical device registration, UK MDR compliance, and regulatory documentation, ensuring your product meets all required standards.
WHAT I OFFER
- MHRA medical device registration (UK)
- UKCA marking and certification guidance
- Medical device classification support (Class I, IIa, IIb, III)
- MDR / UK MDR compliance support
- Declaration of Conformity (DoC) preparation
- Technical file & documentation guidance
- ISO 13485 compliance support
- FDA & EU MDR compliance (optional support)
WHO THIS IS FOR
Medical device manufacturers
Importers & distributors
Startup medical device brands
Amazon & eCommerce sellers
Healthcare product companies
️ WHY THIS IS IMPORTANT
Without proper MHRA registration and UKCA compliance:
- Your product cannot be legally sold in the UK
- Risk of regulatory penalties
- Product seizure or market rejection
- Business delays and losses
I ensure your product meets all compliance requirements
Get to know Viva Lucas
Viva Lucas
Global Regulatory Expert EU, UK, Canada Compliance
- FromUnited States
- Member sinceApr 2026
- Avg. response time1 hour
Languages
English, French, German, Italian
I am a regulatory compliance specialist helping brands meet EU, UK, and Canadian requirements for cosmetics, medical devices, and chemicals. I provide CPNP, SCPN, MHRA, UKCA, NPN, UFI, and PCN submissions with precision and speed. From label review and SDS checks to full dossier preparation, I ensure your products are compliant and market-ready. My focus is accuracy, fast turnaround, and hassle-free approvals so you can scale your business with confidence.
Other Regulatory Compliance Consulting Services I Offer
FAQ
Do I need UKCA marking?
Yes, UKCA marking is mandatory for most medical devices sold in the UK.
What is MHRA registration?
MHRA is the UK authority responsible for regulating medical devices. Registration is required before selling in the UK.
Can you help with technical documentation?
Yes, I assist with technical file, DoC, and compliance documents.
Do you support FDA or EU MDR?
Yes, I can also assist with FDA and EU MDR compliance.
