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Português
$
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I will do mhra registration, ukca certificate, fda registration eu mdr documentation
Catherine
Sobre este Serviço
Planning to launch your medical device in the UK, EU, or USA with full compliance?
You're in the right place.
I am a regulatory affairs consultant specializing in medical device compliance for startups, manufacturers, and exporters. I help clients achieve fast mhra registration, ukca marking, and fda compliance with accurate documentation and smooth approval processes.
Services include mhra registration (UK authority for medical devices), ukca certificates and declarations of conformity, and UK responsible person (UK RP) support. I also handle fda registration, fda documentation, EMA eCTD modules, eu mdr technical file, ce marking, ISO 13485 documentation, and EC certificate of conformity.
I deliver complete compliance for mdr, fda, ukca, and global markets, including technical writing, SOP writing, risk management, GMP, SDS, and product compliance documents.
I also support cosmetics, supplement, and food safety projects such as food registration, food labeling, food compliance, and FSVP agent services.
Message me to get started.
Conheça mais sobre Catherine
Catherine
TOP R
- A partir deEstados Unidos
- Membro desdemar. de 2026
- Responde em aprox.:2 horas
Idiomas
Inglês
I provide accurate translation services along with assistance in handling key documentation such as VAT registration, FDA registration, cpsia, ITIN applications, visa, work permit and form submissions, Duns number, mhra registration, ukca certificate . I support individuals and businesses in completing these processes in a simple and efficient way. My goal is to deliver clear, organized, and high-standard work that is tailored to meet your specific requirements.
Perguntas frequentes
What regulatory services do you provide for medical devices?
I offer mhra registration, ukca marking, fda registration, and full fda compliance support. I also prepare eu mdr technical file, ce marking documents, ISO 13485 documentation, and complete regulatory affairs consulting for medical devices.
Can you help non-UK or international manufacturers enter the UK market?
Yes. I support international clients with mhra registration, uk responsible person (UK RP) services, and ukca certification. I ensure full uk compliance so your medical device meets all regulatory requirements.
Do you provide documentation only or full compliance support?
Both. I deliver technical writing services such as technical file, SOP writing, risk management, GMP, SDS, and fda documentation. I also provide full consulting from registration to product compliance approval.
