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RegulatoryExp
@a_compliancepro
Mpharm
India
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Sobre mí
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.
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RegulatoryExp
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Escritura técnica
I will write or review your pharmaceutical gxp sops and CSV documentation
