NUVO Consultancy is your single point Pharma Regulatory and Project Management resource, servicing the ever growing requirements of the Pharma Generic Industry. NUVO Consultancy offers an efficient and reliable regulatory and quality support, focused especially from the perspective of international requirements. NUVO always aspire to provide an efficient and value added support in obtaining faster Regulatory approvals for our clients. We provide a creative, flexible, dedicated and reliable regulatory and quality centric customer focused pharmaceutical services which are second to none. Already entertaining inquiries into product development and sourcing, NUVO is planning to expand its operations into the said areas. We provide regulatory affairs support as consultants to pharmaceutical companies based across the globe on timely registration of their products globally. NUVO Consultancy was conceptualized by regulatory professionals who have been associated with Pharmaceutical industry with some of the best known pharmaceutical companies for more than a decade with rich and extensive experience in managing regulatory submissions and procedures like DMF and CEP preparation and submission, ANDA submission, regulatory procedures like DCP, MRP, National procedures, Dossier Writing. Apart from managing submissions, the team has profound expertise in but not limited to advising regulatory strategies, Life cycle management, GMP audits, Trainings and Business development. For EU we perform the readability testing, translations of PIL and SmPC, batch release and batch testing at EU site.