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Found 99 results for the keyword edqm. Time 0.007 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.
The Andhra Sugars Ltd - Chemicals Fertilizers Products ManufacturingThe Andhra Sugars Ltd engaged into manufacturing and Exporting of various Chemicals Fertilizers Products. Our factory has various Certifications such as GMP, ISO 9001 : 2008 and approved by USFDA EDQM.
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.
PharmaOutlook | Latest Pharma Articles - India Pharma OutlookDive into the world of pharmaceuticals. Discover cutting-edge insights, trends, and breakthroughs shaping the industry today.
Masuu US Agent: Pre-Assigned Application Numbers TrackingMasuu US Agent aids foreign pharma in obtaining pre-assigned application numbers (ANDA, NDA, BLA) via the USFDA’s CDER NextGen portal for smooth tracking.
Language Translation service, Native language translatorsMasuu Global provides accurate, culturally resonant language translation for diverse industries in Spanish, German, Russian, Chinese more,
Expert Toxicologists for Detailed PDE, OEL OEB Value ReportsMasuu Global’s toxicologists offer precise PDE, OEL OEB value reports with thorough literature searches, ensuring compliance and approval.
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.
Regulatory support services, Associate Regulatory Services, RegulatoryMasuu offers expert regulatory support services, ensuring compliance and efficiency. Trust us for comprehensive solutions tailored to your needs.
eCTD Software, eCTD Publishing tool, eCTD Submission softwareMasuu Global s NextGen eCTD software is an eCTD Software tool, that streamlines creation, validation, publishing, viewing, and reporting of electronic regulatory submissions to ensure compliance with global Health Author
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