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If you are demanding any product or service please register as Farmavita.Net network member and publish your offer or demad. In-Licensing and oursoucing of products is usual a way for development of winning portfolio of products. License-in is also very cost effective way of product/technology development. Opportunities are listed according chronological order, the most recent first.

Regulatory Affairs

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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
Pharmaceutical Dossier Documents service
Please contact me.  if you need pharmaceutical Registration dossier and documents service

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