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.
At NUVO, we offer our clients highly professional and effective services to all of their 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 all types of electronic
submissions and other special requirements.
For our clients, we always aspire to provide an efficient and value added support In obtaining
NUVO has rich and extensive experience in managing regulatory submissions and procedures like
DMF and CEP preparation and submission, ANDA submission, European filings via regulatory
procedures like DCP, MRP, National procedures, Dossier Writing for global markets. Apart from
managing submissions, the team has profound expertise in but not limited to devising regulatory
strategies, Life cycle management, GMP audits, Trainings and Business development.