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English
$
USD
I will handle mhra registration, ukca and medical device compliance
FDA Registration Regulatory Compliance Specialist
My name is Sarah Via. I help businesses with FDA registration, U.S. Agent requirements, FSVP support, food facility registration, product and label compliance, and UK medical-device requirements. I pr...
About this Gig
Are you a medical device manufacturer looking to enter or sell in the UK market?
I provide practical MHRA registration, UKCA compliance, UK Responsible Person (UKRP), and medical device documentation support to help you understand and organize your UK regulatory requirements.
My services include:
- MHRA medical device registration support
- UKCA compliance assessment
- UK Responsible Person (UKRP) guidance
- Medical device documentation review
- Technical documentation review
- UK medical device labeling review
- Regulatory requirements assessment
- Compliance gap identification
- UK market entry guidance
- Documentation and submission support
I can work with manufacturers and businesses dealing with applicable medical devices and help you understand the regulatory steps relevant to your product.
Whether you are preparing to enter the UK market, reviewing an existing registration, or checking your documentation for compliance gaps, I will assess your requirements and provide practical next steps.
Please message me before ordering with your device type, manufacturer location, intended UK market, and the specific regulatory service you need.
Type of Business:
LLC
•
C-corp
Target country:
Worldwide
•
United Kingdom
•
United States
Service type:
Registered agent services
•
Compliance monitoring
Business formation & registration Gigs are not screened
Fiverr does not pre-screen freelancers offering services in Business Formation & Registration. We advise thoroughly reviewing freelancer profiles, asking questions, and confirming their qualifications to ensure they meet your requirements. Freelancers marked as “Pro” have completed a vetting process for added confidence. Learn more here.
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FAQ
Can you help foreign manufacturers register medical devices with the MHRA?
Yes. I can assist foreign manufacturers with the MHRA registration process, required information, documentation, and submission preparation.
Do you provide UK Responsible Person (UKRP) support?
Yes, where applicable. I can provide guidance on UKRP requirements and help you understand the responsibilities and documentation involved.
Can you review my UKCA technical documentation?
Yes. I can review your available technical documentation and identify potential compliance gaps or areas that may need attention.
Can you help with UKCA medical device compliance?
Yes. I can assess your product against the applicable UK regulatory requirements and provide practical guidance on the documentation and compliance steps involved.
What information do you need before starting?
Please provide your device name and type, manufacturer location, intended UK market, current regulatory status, and any existing MHRA, UKCA, UKRP, or technical documentation you have.
