Regulatory Affairs

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GxP audits (GMP,GDP, GLP, GCP,etc.), facility feasibility audits, GAP analysis audits, supply security audits,computer system validations and CVS audits, GxP training
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Dossier comiplation, dossier review, dossier submission, registration services in EU and MENA, Pharmacovigilance, product development, tech transfers and scale-ups, facility design and upgrading
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Please contact me.  if you need pharmaceutical Registration dossier and documents service

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