August 2011
Complimentary Webinar • Government Pricing Automation: The Time is Now
August 10 2011-August 9, 2012
A Look Into the Future: Ophthalmic Capabilities in Drug Discovery and Toxicology
August 30 2011-August 29, 2012
September 2011
Patient Reported Outcome (PRO) Assessments in Clinical Trials: Navigating the EMA and FDA Regulatory Framework
September 22 2011-September 21, 2012
In Search of the Perfect PK-PD Relationship: Finding the Bridge to the Ideal Pharmacodynamic Response
September 29 2011-September 28, 2012
October 2011
Cellular Therapeutics and Regenerative Medicine: Preclinical Assessments for Proof of Concept and Safety
October 11 2011-October 10, 2012
Innovative Technologies to Improve Data Quality in CNS Clinical Trials
October 12 2011-October 11, 2012
Determine Total Cost of Ownership and Minimize Risk of Reprints Spend
October 18 2011-October 17, 2012
The Future of Wireless Medical Devices – FCC, FDA and Patent Considerations
October 25 2011-October 24, 2012
Final Gap Analysis of Aggregate Spend Processes and Systems for 2012 Collection
October 27 2011-October 26, 2012
November 2011
Meeting the Challenge of Increased Regulatory Focus on Chromatography Data Systems
November 10 2011-November 9, 2012
Take Control of Patient Communication, Reduce Missing Data and Maximize Compliance and Retention
November 10 2011-November 9, 2012
New Developments in Source and Mass Spec Technology Reducing Sample Prep
November 14 2011-November 13, 2012
Out of Specification (OOS) Investigations for GLP Nonclinical Studies
November 15 2011-November 14, 2012
Trial Regulatory Document Management: Balance Through Best Practice
November 16 2011-November 15, 2012
Multi-Faceted Registries: Not Your Typical Safety or Pregnancy Exposure Registry
November 30 2011-December 1, 2012
December 2011
