|Event Name||CFPIE 2012 Clinical Document Management - A Trial by Trial Approach to Compliance
Thursday, November 01, 2012
Friday, November 02, 2012
|Description||By the end of this two-day session, attendees will understand the varied documentation requirements of global clinical trials and be able to assess documentation needs in the context of electronic, paper or hybrid systems. Additionally, participants will develop a firm understanding of the roles and responsibilities of sites, sponsors, CROs and other stakeholders in relation to clinical documentation. Development of Standard Operating Procedures (SOPs), the Trial Master File and conducting compliant audits will also be given significant attention.