Pharma companies today face the challenge to sharpen their interface with Doctors amidst declining ‘brand recall’ and heavy premium on ‘face time’. Companies require abilities to influence key doctors and manage their Customer relationships in an effective manner . If you would like to know more about how to achieve this objective……… click here

Data is the fundamental residual asset from conducting a trial. It forms the core of drug approval process. A myriad of activities need to be managed efficiently to arrive at clean and validated data. Calyx eData Capture solution enables an organisation to manage all this comfortably and accurately. ………….click here

Clinical Trial Management is fundamentally a project management requirement. Tracking and managing Events, Documents, Approvals and Clearances, Monitoring Activities, Site Enrolments, Agreements and Contracts, Resource availability and Scheduling, are the tasks to be handled under Clinical Trial Management. To know more about Calyx solution in this area………….click here

Conducting of bioequivalence studies can be quick, easy and programming-free. All study related activities from Volunteer Registration and Enrolment to Final Study Analysis and Closure will be carried out through an extremely user friendly computerised system. To learn more about Calyx solution for Bio Equivalence study handling………….click here

Patient registries  provide a collaborative working environment for maintaining patient information, analyzing and studying patterns and treatment efficacy. It also allows users to draw summary information across the global patient database and specific patient history for publication purposes. Calyx has developed and implemented multiple registries to date. To know more…………. click here