Who should attend?




This event will particularly benefit professionals involved in the planning, logistics, management and implementation of e-clinical trials. It will introduce new e-clinical professionals to the entire scope of their responsibilities, and upgrade the knowledge base of experienced clinical supply professionals with new technologies and processes.

  Senior representatives from biotech, pharmaceutical companies and CRO’s working within the following areas::
   
 
  • Clinical Trials
  • Clinical Data Manager
  • Clinical Operations
  • Clinical Development
  • Monitoring Systems
  • Clinical Research
  • EDC
  • Clinical Information Management
  • Medical Information Systems
  • CDISC
  • CTMS
  • Pharmacovigilence
  • Clinical QA
  • Regulatory Affairs
  • Clinical Project Management
  • Clinical Auditors
  • Heads of Quality Control/Assurance/GCP
  • Compliance
  • Clinical Statisticians
  • Programmers