Zifo Technologies is a Specialised Research Data Management Service provider. We leverage specialised services in Clinical Data Solutions, Discovery & Lab Informatics and Technology Services for regulated environment. A deep understanding of the research industry and our technological expertise enables us to meet the toughest challenges of the Bio-Pharma companies (Pharmaceutical, Bio-technology, Medical Devices), Contract Research Organisations and Product companies. Zifo is headquartered in the metropolitan city of Chennai, the capital city of the state of Tamil Nadu, in the southern part of India. We cater to a global customer base comprising of leading Bio-Pharma companies across various parts of US, UK, Europe and Asia. Our employees are our biggest asset. The strong foundation of the Zifo Team comprises of best-in-class leaders who have the know-how and experience in the Bio-Pharma industry (and Life Sciences domain, in general) and detailed knowledge on international regulatory compliance. Our employees bring forward the blend of knowledge and skill, in understanding and implementing new technology and tools which add tremendous value to our processes and service delivery. The Quality Management System in Zifo is ISO 9001:2008 compliant and is based on ISO/TR 10013:2001, ISO/IEC 90003:2004, FDA 21 CFR Part 820 and GxP. As we work primarily for customers functioning in regulated environments, EU-Annex 11, GAMP 5 and FDA 21 CFR Part 11 have been appropriately considered in defining Zifo’s QMS. Our IT infrastructure is robust and compliant. Zifo is vendor-neutral and provides technology solutions across various software and hardware platforms. Our zeal for intensive focus in all aspects of service including quality, timeline, cost and value additions, support our aim to make an impact on healthcare and human life.
