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Found 21569 results for any of the keywords eu ema edqm. Time 0.012 seconds.
EU EMA/EDQM SPOR ID Registration and ComplianceMasuu Global offers expert help for ORG_ID and LOC_ID registration in SPOR, ensuring EU EMA/EDQM compliance and efficiency.
Expert EU MAH QP Services for Pharma, MAH Services, EU QPMasuu Global provides EU MAH QP services, including audit support, dossier filing, and regulatory compliance for pharma companies.
Medical Devices Regulatory Services , MDV Regulatory ConsultingMasuu offers regulatory and quality services for medical devices, ensuring compliance with global standards like FDA, EMA, and ISO 13485.
Post inspection remediation, Regulatory remediation servicesMASUU Global ais pharma with post-inspection remediation, identifying causes corrective actions for FDA, EMA health authority compliance.
Computer System Validation, Computer System Validation ServicesMASUU Global offers Computer System Validation (CSV) for pharma biotech, ensuring data integrity, system reliability FDA/EMA compliance.
Upgradation of Domestic Site to Regulatory , Site UpgradationMASUU provides guidance for site upgrade to regulatory standard. Ensure FDA, EMA, and global compliance with gap assessments and training.
Package Inserts (PIs) and SmPCs Regulatory Labeling ServicesMasuu Global offers expert regulatory labeling for Package Inserts (PIs) SmPCs, ensuring global compliance with FDA, EMA, TGA, and more.
GxP Audit, GxP audit services, GxP audit solution, GxP ComplianceMasuu Global offers modern GxP audit services for life sciences, ensuring flexible, top-quality compliance with global industry standards.
Regulatory Review, Authoring Dossier Compilation ServicesMasuu Global s regulatory review, authoring, and dossier compilation services for global health authorities, including US ANDA, NDA, BLA more.
Regulatory support for Pharma Research Development (R D)Masuu Global supports Pharma Research Development (R D) with expert regulatory, quality, and compliance services from preclinical to market.
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