NUVO

At NUVO, we offer our clients highly professional and effective services to all of their Pharma and Regulatory requirements. We also provide expert procedural and technical guidance to our clients so as to manage complex regulatory procedures efficiently. We provide service for eCTD publishing and submissions and other special requirements... NUVO has rich and extensive experience in managing regulatory submissions and procedures. NUVO deliver quality module preparation and submission with eCTD Publishing of DMF, CEP for EDQM via CESP, ANDA 505j & 505b(1)(2), European filings via regulatory procedures like DCP, MRP, National procedures, WHO prequalification, China filings and other CTD filings across the globe. Apart from managing submissions, the team has profound expertise in but not limited to devising regulatory strategies, module writing for DMF and Dossiers, Life cycle management, GMP audits, Trainings, It solutions for Healthcare and pharmaceutical industry and Pharma support..

Also known as: Nuvo Consultancy

Primary location: Sacramento United States