Regulatory Affairs Consulting Services, Regulatory Affairs Services, Consultants

Masuu Global provides global regulatory affairs consulting services to pharmaceutical, biotech, and biomedical companies to comply with regulatory requirements of health authorities worldwide.
Masuu Global Solutions which is based in the USA and India and providing end to end Regulatory Affairs (Dossier Compilation in CTD, ACTD, NeeS, eCTD and Country Specific Format), Regulatory Operations (eCTD and NeeS, Document Level Publishing, Submission Level Publishing and Submission Management), Regulatory Labeling (Labeling Content and Artwork Development) and Structured Product Labeling (SPL i.e. ER, NDC Labeler Code, Drug Listing and GDUFA Self Identification) services to Pharmaceuticals, Biopharmaceuticals, Healthcare and Life Sciences industry across the globe.