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I will register your medical device with mhra for UK compliance
Brian Collins
About this gig
Get Your Medical Device MHRA Registered and UKCA Compliant Fast
Selling a medical device in the UK without MHRA registration is illegal.
One wrong classification or missing file is all it takes for MHRA to reject your submission, freeze your product at customs, or delay your launch by months. Every week without compliance costs you revenue and market share.
Most sellers get lost in the DORS portal, misclassify their device, or hire freelancers using generic templates that don't match UK MDR 2002. They end up starting over.
I handle your MHRA registration and UKCA compliance, done right the first time.
What you get:
- Accurate device classification under UK MDR 2002
- Complete MHRA DORS portal registration
- UKCA Declaration of Conformity
- Technical file review to close compliance gaps
- Guidance on appointing your UK Responsible Person
You get an audit ready submission and a clear path to legally sell your device in the UK, without delays or rejections.
Message me your device type now, let's get your registration moving today.
Get to know Brian Collins
Brian Collins
Regulatory Compliance Specialist, MHRA, UKCA, CPNP and SCPN Documentation Expert
- FromUnited States
- Member sinceApr 2026
- Avg. response time1 hour
Languages
English, French, German
Launching a medical device or cosmetic product in the UK and EU?
One compliance gap can mean instant MHRA rejection, a blocked cosmetic listing, or a shipment frozen at customs. I help manufacturers, importers, and startups get MHRA registered, UKCA compliant, and CPNP/SCPN notified accurately, without guesswork or delays.
You get correct classification, clean documentation, and submissions built to pass, so your product reaches buyers on schedule instead of stuck in review.
Message me with your product type and let's map out your compliance path today.
Other Regulatory Compliance Consulting Services I Offer
FAQ
Do you register medical devices with MHRA?
Yes, I handle your full MHRA DORS registration and classification.
Do I still need a UK Responsible Person?
Yes, it's a legal requirement. I can find and appoint one for you.
How long does MHRA registration take?
Delivery is 3-7 days depending on your package; MHRA's own review adds extra time.
Do you guarantee approval?
I guarantee an accurate, compliant submission. Final approval is MHRA's decision.
What device classes do you handle?
Class I, IIa, IIb, and III under UK MDR 2002.
Can you review my existing technical file?
Yes, that's included from the Standard package up.
Do you handle UKCA marking too?
Yes, UKCA Declaration of Conformity is included in Standard and Premium.
What do you need from me to start?
Your device type, intended use, and any existing documentation.
Can you work with non-UK manufacturers?
Yes, that's exactly who this service is built for.
Why message before ordering?
So I can confirm your device classification and recommend the right package.
