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Maryam
@maryleaf
Level 2
Certified Regulatory Affairs Professional for Medical Industry
United States
English
About me
I am a dedicated medical devices expert with extensive experience in all aspects of laws, standards, regulations, directives, and guidelines related to the medical devices industry. I specialize in navigating global regulatory frameworks, I specialize in navigating complex regulatory landscapes, including ISO, CE MARK, MDR, FDA, EMA, TGA, and ECREP, SFDA, etc. With expertise of decades I help clients achieve regulatory compliance and market access for their medical devices. My services include regulatory strategy, technical documentation, regulatory submissions, and post-market surveillance.
Skills
Maryam
Offline •
Average response time: 1 hour
See my services
Medical Device Regulatory
I will iso 13485 consulting and certification preparation for medical devices
IT & Cybersecurity Certification
I will achieve iso 9001 certification with efficient qms
Portfolio
159 Reviews
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Rating Breakdown
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- Quality of delivery
- Value of delivery
1-5 out of 159 Reviews
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awenckebach
Repeat Client
Switzerland
Fast and efficeint, in summary very good work. We are now engage Myryam on a more sustained work, and looking forward to the next phases of work.
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awenckebach
Repeat Client
Switzerland
Maryam reacted quite fast to address our gaps in the ISO 13485 process. Efficient
Seller's Response
Helpful?
andremoreira04
Portugal
Helpful?
mary_gonzales1
United States
Very satisfied with the service. The seller delivered a polished result and maintained a professional workflow throughout.
Helpful?
willardadk
United States
The seller showed strong attention to detail and a clear understanding of the project objectives.
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