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English
$
USD
I will handle your mhra registration and ukrp representation
Evelyn Robbins
About this gig
SECURE YOUR UK MARKET ACCESS WITH EXPERT MHRA REGISTRATION SERVICES
Selling MEDICAL DEVICES in the UK without proper registration isn't just DIFFICULT IT'S ILLEGAL. One minor clerical error in your technical file can lead to REJECTED APPLICATION, CUSTOMS SEIZURES, and thousands in LOST REVENUE.
The UK regulatory landscape changed after BREXIT, and trying to handle it alone often leads to months of frustrating delays and missed sales opportunities.
Stop risking your business reputation.
I provide the professional interference you need to bypass these hurdles. I handle your entire MHRA REGISTRATION process, ensuring every document meets strict UKCA and MDR requirements. By managing your UKRP representation and device listing, I offer a seamless path to compliance.
You get guaranteed accuracy, faster market entry, and the peace of mind that your products are legally protected. No more regulatory headaches; just a clear, compliant path to selling in the UK. Let's get your medical devices registered and ready for profit.
Are you struggling to navigate the complex MHRA DORS portal?
MESSAGE ME NOW TO CONFIRM YOUR DEVICE CLASS AND START YOUR REGISTRATION.
Get to know Evelyn Robbins
Evelyn Robbins
Regulatory Affairs Compliance Specialist
- FromUnited Kingdom
- Member sinceMay 2026
- Avg. response time1 hour
Languages
English, Spanish, French, German
Stop risking your UK market entry with regulatory delays. As an expert MHRA consultant, I specialize in seamless medical device and IVD registrations for global manufacturers and UKRPs. I handle the complex technical documentation and DORS portal submissions so you can focus on scaling your business. My clients gain peace of mind, guaranteed compliance, and rapid 24-hour processing to avoid costly border rejections. Ready to authorize your products for the UK market?
Message me today to secure your MHRA registration and start selling
FAQ
What information do I need to start my MHRA registration?
You need your device classification, GMDN codes, and technical documentation ready for review to ensure a smooth submission.
Can a NON-UK manufacturer register directly with the MHRA?
No. If you are outside the UK, you MUST appoint a UK Responsible Person (UKRP) to handle the registration on your behalf.
How long does the MHRA registration process actually take?
While I complete the submission within days, the MHRA usually takes 5 to 10 working days to process and issue your confirmation.
Does this gig include the MHRA statutory fees?
No. My fee covers professional consulting and submission. You must pay the MHRA statutory fee separately via their portal.
Will you help with UKCA marking requirements?
Yes. I ensure your MHRA registration aligns with current UKCA marking standards for medical devices and IVDs.
Do you handle Class I, II, and III medical devices?
Absolutely. I am experienced in the specific documentation required for all device classes, including IVDs and custom-made devices.
What happens if my registration is rejected?
By using my service, you minimize this risk. I pre-screen your documents to ensure they meet MHRA standards before we hit submit.
Can you act as my UK Responsible Person (UKRP)?
Yes, my Premium package is designed specifically for international manufacturers who need a legal UK representative.
Is MHRA registration mandatory for all medical devices?
Yes. To legally place any medical device on the Great Britain market, it must be registered with the MHRA.
Can you update an existing MHRA registration?
Yes. If you need to add new products or update manufacturer details on an existing account, I can manage that for you.
