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Maissa
@assia_em
Medical Device Regulatory Affairs : FDA Labeling and Technical Documentation
Algeria
Arabic, English, French
About me
Pharmaceutical and medical device professional with experience in Regulatory Affairs, CMC, Quality and GMP. Familiar with drug products, APIs, excipients, formulations, manufacturing processes, CTAs and regulatory writing. Medical device experience includes FDA requirements, labeling, UDI, post market activities, CAPA, NCRs and technical documentation. Fluent in French, English and Arabic, with experience in translation and transcription. I provide regulatory research, technical and scientific writing, documentation support, and specialized medical and pharmaceutical translation.
Skills
Maissa
Offline •
Average response time: 38 hours
See my services
Technical Writing
I will write gmp sops, quality documents and procedures
Technical Writing
I will perform a medical device regulatory gap analysis and compliance review
7 Reviews
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Rating Breakdown
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1-5 out of 7 Reviews
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gmpeeo
Czech Republic
Ongoing collaboration
Assia understands her field. She is professional, easy to work with, punctual, and always meets the expectations.
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tomalicki
Saudi Arabia
Helpful?
gmpeeo
Czech Republic
Ongoing collaboration
Assia is a professional and knowledgeable about the subject. Easy to work with.
Helpful?
gmpeeo
Czech Republic
Ongoing collaboration
Seller's Response
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bferguson356
United States
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