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Explorer
Fiverr Pro
Français
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RegulatoryExp
@a_compliancepro
Mpharm
Inde
Anglais
À propos de moi
I am a Post graduate M. Pharma Proffesional and Regulatory Affairs specialist with extensive experience reviewing technical data against international standards. I specialize in bridging the gap between raw pharmaceutical workflows and strict regulatory frameworks like USFDA 21 CFR Part 11, GAMP 5, and ALCOA+ Data Integrity. I transform raw laboratory notes, workflows, or bullet points into clear, structured, and audit-ready documentation.
Compétences
RegulatoryExp
hors ligne •
Voir mes services
Rédaction technique
I will write or review your pharmaceutical gxp sops and CSV documentation
