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I am a Regulatory Affairs professional with hands-on experience of around 7 years in preparing high-quality pharmaceutical dossiers in compliance with DRAP for registration of local and import pharmaceutical amd nutraceutical products.
In addition to this, can prepare documents for all regulatory submissions, PRVs and other
DRAP correspondence.... Mehr lesen
m
Mahaali
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Technische Texte
I will ctd dossier and drug registration correspondence