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rachelsuccess46

Mhra Reg

@rachelsuccess46

Medical Device Regulatory Affairs Specialist FDA CE MHRA and ISO Compliance

United Kingdom
English, German, Spanish
About me
I am a Medical Device Regulatory Affairs Specialist helping manufacturers and businesses achieve FDA, CE, MHRA, UKCA, and ISO compliance. I specialize in FDA establishment registration, medical device listing, CE documentation, MHRA registration, UKCA requirements, and ISO compliance guidance. I deliver accurate regulatory support, clear documentation, and practical solutions to help you avoid delays, meet compliance requirements, and bring your medical devices to market with confidence.... Read more

Skills

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rachelsuccess46
Mhra Reg
Offline • 
Average response time: 11 hours

See my services

Medical Device Regulatory
I will register your medical device with mhra and ensure UK compliance
From$30 / projectMore details
Product Safety & Quality Certification
I will register your medical device with mhra and ensure UK compliance
From$20 / projectMore details

Work experience

Fiverr

Medical Device Regulatory Affairs Specialist

Fiverr • Self-employed

Sep 2025 - Present • 10 mos

I provide regulatory consulting services for medical device manufacturers, importers, and distributors. My expertise includes FDA Establishment Registration and Device Listing, MHRA Registration, CE compliance documentation, UKCA requirements, ISO 13485 guidance, Declaration of Conformity preparation, and regulatory documentation. I help clients meet compliance requirements, avoid regulatory delays, and prepare products for market entry.