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Category about in-license needs for generic medicines. Please contact us for details about the authors of offers. Register as the network member. Members are invited to publish their needs, for free.

Regulatory Affairs

GxP audits-Key Starting Materials qualification-Regulatory services
GxP audits (GMP,GDP, GLP, GCP,etc.), facility feasibility audits, GAP analysis audits, supply security audits,computer system validations and CVS audits, GxP training
Regulatory affairs, CEP Application, registration services in EU and MENA, Technical transfers
Dossier comiplation, dossier review, dossier submission, registration services in EU and MENA, Pharmacovigilance, product development, tech transfers and scale-ups, facility design and upgrading

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