Regulatory Affairs

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

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