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Maissa
@assia_em
Medical Device Regulatory Affairs : FDA Labeling and Technical Documentation
Algérie
Arabe, Anglais, Français
À propos de moi
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.
Compétences
Maissa
hors ligne •
Temps de réponse moyen de 38 heures
Voir mes services
Rédaction technique
I will write gmp sops, quality documents and procedures
Rédaction technique
I will perform a medical device regulatory gap analysis and compliance review
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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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gmpeeo
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Assia is a professional and knowledgeable about the subject. Easy to work with.
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