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Found 224 results for any of the keywords biosimilars companies. Time 0.009 seconds.
Regulatory Support for Pharma Biosimilars CompaniesMasuu offers regulatory support for biosimilars, including strategy, comparability studies, dossier submission, post-approval surveillance.
Contract Development and Manufacturing Organization (CDMO)Partner with Masuu Global for regulatory submissions, quality management compliance to elevate your Pharma Contract Development and Manufacturing Organization operations.
Contract Manufacturing Organization (CMO), Pharma CMOPartner with Masuu Global for tailored regulatory quality services for Contract Manufacturing Organization, ensuring GMP compliance manufacturing integrity.
Clinical Research Organization, Clinical Research OperationsPartner with Masuu Global, a top clinical research organization, for regulatory consulting, compliance audits quality management solutions.
Active Pharmaceutical Ingredients (APIs), Quality APIMasuu Global s Active Pharmaceutical Ingredients (APIs), offering expert development, GMP audits, and lifecycle management for top quality.
Pharmaceutical Raw Material and IntermediatesMasuu Global s pharmaceutical raw material intermediates, including APIs and excipients. Ensure quality compliance with our expert support
Regulatory and Quality Services for Pharma ExcipientsMasuu Global offers premium pharma excipients with regulatory and quality services, including supplier qualification and risk assessment.
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.
Drug and Biologics Formulation, Pharma FormulationMasuu Global specializes in drug and biologics formulation with regulatory support, stability studies GMP compliance for effective products.
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.
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