Sfoglia categorie
Esplora
Fiverr Pro
Italiano
$
USD
Maissa
@assia_em
Medical Device Regulatory Affairs : FDA Labeling and Technical Documentation
Algeria
Arabo, Inglese, Francese
Chi sono
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.
Competenze
Maissa
offline •
Tempo di risposta medio: 38 ore
Consulta i miei servizi
Scrittura tecnica
I will write gmp sops, quality documents and procedures
Scrittura tecnica
I will perform a medical device regulatory gap analysis and compliance review
7 Recensioni
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Valutazione dettagliata
- Livello di comunicazione del venditore
- Qualità della consegna
- Valore della consegna
1-5 di 7 recensioni
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Più rilevante
gmpeeo
Repubblica Ceca
Collaborazione in corso
Assia understands her field. She is professional, easy to work with, punctual, and always meets the expectations.
Risposta del venditore
Utile?
tomalicki
Arabia Saudita
Utile?
gmpeeo
Repubblica Ceca
Collaborazione in corso
Assia is a professional and knowledgeable about the subject. Easy to work with.
Utile?
gmpeeo
Repubblica Ceca
Collaborazione in corso
Risposta del venditore
Utile?
bferguson356
Stati Uniti
Utile?
