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Nederlands
$
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Maissa
@assia_em
Medical Device Regulatory Affairs : FDA Labeling and Technical Documentation
Algerije
Arabisch, Engels, Frans
Over mij
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.
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Maissa
offline •
Gemiddelde reactietijd: 38 uur
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Technische teksten
I will write gmp sops, quality documents and procedures
Technische teksten
I will perform a medical device regulatory gap analysis and compliance review
7 Reviews
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gmpeeo
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Assia understands her field. She is professional, easy to work with, punctual, and always meets the expectations.
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tomalicki
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gmpeeo
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Assia is a professional and knowledgeable about the subject. Easy to work with.
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gmpeeo
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