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Found 1582 results for any of the keywords product dossier. Time 0.020 seconds.
RA.Pro CTD, ACTD, eCTD & Country Specific Dossier SoftwareAll-in-one CTD, ACTD, eCTD and Country Specific Dossier Preparation Software. Simplify Dossier Preparation, Regulatory Publishing and RIMS management.
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.
Software Development, Website Development and Mobile App DevelopmentWebsite Design & Development, Software Development, mobile application development. Rosix Technology Pvt Ltd Ahmedabad (Gujarat) India.
Medical Writing | Medical Writing Services | QPlusConsultAn increasing number of research studies and growing clinical experience result in new knowledge and information on medicinal products, medical devices,
Software Development, Website Development and Mobile App DevelopmentWebsite Design & Development, Software Development, mobile application development. Rosix Technology Pvt Ltd Ahmedabad (Gujarat) India.
Software Development, Website Development and Mobile App DevelopmentWebsite Design & Development, Software Development, mobile application development. Rosix Technology Pvt Ltd Ahmedabad (Gujarat) India.
Regulatory Strategy, Dossier Filing, Regulatory Strategy ServicesMasuu Global: Custom Regulatory Strategy Dossier Filing for Successful Global Drug Product Submissions and Market Entry
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.
Dossier Lifecycle Management, Pharma Lifecycle ManagementMasuu Global supports drug development, approval, and dossier lifecycle management, ensuring efficient and smooth regulatory submissions.
DUNS Number registration, DUNS Number, DUNS RegistrationMasuu US Agent specializes in DUNS number registration, helping pharma firms obtain or update numbers for efficient USFDA compliance.
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