ISCR



Conference Overview
Indian Society for Clinical Research brings you the 2nd edition of its annual conference – an exclusive scientific convention for all clinical research personnel in India – with excellent topics in each of the sessions in the main 2-day conference on January 11-12, 2009. The 2-day annual scientific conference has become an annual event for all stakeholders in clinical research for professional development and networking. This year’s conference will have 3 tracks - Clinical Research, Clinical Data Management and Biostatistics & Medical Writing tracks running in parallel. A full day pre-conference workshop – “Study Data Tabulation Model (SDTM) from CDISC” – has been arranged on Saturday 10, January 2009. This workshop is intended for those who wish to have a practical introduction to SDTM standard of CDISC. It will be useful for those working in clinical data management and statistical programming domain and are involved in or planning SDTM implementation activities. Post-conference workshop – on January 13, 2009 – To be announced.
Conference Objectives
The objective of the conference is to provide a forum for sharing experiences, for professional advancement of the participants, understanding the policy environment locally & globally and to provide a platform for developing relationships and explore new partnership opportunities. The scientific programme has 4 sessions of 1.5 hours in each track per day totaling 8 sessions for the 2-day conference. Each session will discuss updates on three focused topics through national & International subject matter experts. [Please go to “Event Information” link to get details of all topics under respective tracks.] This first-of-a-kind exclusive conference for the clinical research industry in India organized by Indian Society for Clinical Research is gaining a reputation of a must-attend conference for networking with all major players of the industry in these two days.
Who should attend
Academia, Biostatisticians, CROs, Clinical R&D, Clinical Trials, Study Monitoring, and Project Management personnel; Clinical Data Management, Investigators/Site Management, QA / Compliance, Regulatory/Medical/Scientific Affairs personnel.