The Trial Master File Summit 2012 covers topics such as:
The Trial Master File Summit 2012 brings together executives from Pharma, Biotech, and Med Device companies involved in Document Management, Clinical Operations, TMF, Regulatory Affairs, Clinical Development, Clinical Document Coordinator, Regulatory Affairs, Regulatory Operations, Essential Document Management, Program Managers, Quality Assurance, Product Managers, Auditing, Quantitative Operations, Strategic Operations and Planning, Global Planning & Standards, Project Management, Study Delivery, Knowledge Management, Data Management, Clinical Trial Coordinators/Associates, Records Management, CRAs, Clinical Trial Managers, Archives, Information Management, Quality Management, Submission Management, Legal, Informatics and Clinical IT.
