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Subject DepartmentIndustryDate
*Developing a Sampling Plan for Quality Audits Quality Medical Devices Various
Post-Approval Human Factors – Mining Post-Market Reports for Usability Issues Engineering/R&D Medical Devices 24 Apr 2014
*ISO 10993-12 Sample Preparation and Reference Materials Regulatory Medical Devices Various
*Preparing to Implement a Content Management System Training/Learning & Development All Various
*Improving Study Feasibility – Why Sites Fail and How to Avoid It Clinical Pharmaceuticals Various
*Are Your Suppliers Qualified? Prove It. Purchasing Pharmaceuticals Various
*Supporting Investigator-initiated Clinical Trials Clinical Pharmaceuticals Various
*The DOJ/SEC Resource Guide on the FCPA: Considerations for Government Contractors Legal All Various
*Avoiding and Managing Workplace Whistleblower Claims Legal All Various
*Monitoring and Measuring Customer Satisfaction Using ISO 10004:2012 Quality Medical Devices Various

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