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Adaptive/Novel Designs in Oncology: Overview & Issues $249.00 John Constant		Best Practices for Conducting Ophthalmology Trials $249.00 Helen Colquhoun		Best Practices for Literature Reviews, Clinical Evidence Reports and Clinical Study Reports $249.00 Joy Frestedt
Best Practices for Preparing Clinical Evaluation Reports $249.00 Phil Triolo		Clinical Data Requirements Under the New MDD & AIMDD $249.00 Joy Frestedt		Conducting Clinical Evaluations to Support Regulatory Approval and Marketing of Medical Devices $249.00 Janette Benaddi
Conducting Medical Device Studies in the UK $249.00 Janette Benaddi		Conducting Medical Device Studies Under the Revised ISO 14155 $249.00 Janette Benaddi		Considering Human Factors in Designing Medical Device Trials $249.00 Annette Valles-Sukkar
Data Management for Medical Device Trials: Best Practices $249.00 Helen Colquhoun		Developments, Trends and the Future of Neurological Devices $249.00 Jessica Swartz		Effective Strategies for Successful Medical Device-CRO Partnerships in Post-Approval Studies $249.00 Yvonne Albright and Barbara Vargas
Electronic vs. Paper Data Capture: Which Option is Best for Your Trial? $249.00 Helen Colquhoun		GCP for Medical Device Trials: Upcoming Revisions to ISO 14155 $249.00 Carol Houts		Global Clinical Trials & ISO 14155: 2011 Compliance - Are Your Quality Systems Up to Date? $249.00 Joy Frestedt

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