Clinical Data Management By:- Upendra Agrawal 1 Clinical Data Management 2 Content Clinical Data Management (CDM) is a critical phase in clinical research, which leads…
1. Kevin WeatherwaxMICHR IND/IDE InvestigatorAssistance Program (MIAP)September 24, 2014Photo by Jean Guichard 2. The Regulatory Environment can seem like theBay of Fundy…Constantly…
1. Yorkshire Cancer Research Network Annual Work Programme 2009-2010 Published: March 2009 Review Date: March 2010 Yorkshire Cancer Research Network 6th Floor Bexley Wing…
1. FORUM PATIENT ENGAGEMENT IN HEALTH ECONOMIC AND OUTCOMES RESEARCH: CURRENT AND FUTURE ISPOR INITIATIVES 2. Moderator FORUM Todd Berner, MD Co-Chair Patient Engagement…
doi:10.1182/blood-2007-06-093906 Prepublished online Jan 23, 2008; Hartmut Dohner, Peter Hillmen, Michael J. Keating, Emili Montserrat, Kanti R. Rai and Thomas J. Kipps Michael…
1. Risk Based Monitoring – A holistic approach to late phase studies Thursday, May 16, 2013 2. About ICON • ICON plc is a global provider of outsourced development services…
Slide 1An overview of the harmonization of the Common Terminology Criteria for Adverse Events (CTCAE) with the Medical Dictionary for Regulatory Activities (MedDRA) CTCAE…
Slide 1 USF Research Integrity & Compliance eIRB Comprehensive Training 10/07/2014 Slide 2 What is ARC? ARC (Applications for Research Compliance) – Electronic system…
Slide 1 Research Governance Toolkit The journey thus far Bill Karanatsios 20 May 2010 Slide 2 VMIA VMIA is the insurer and risk management advisor for the state of Victoria.…