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Subject DepartmentIndustryDate
*eLabeling in Europe – How to Start and What to Expect from Notified Bodies Labeling/Packaging Medical Devices Various
*Medical Device Reporting (MDR) Requirements – the FDA Draft Guidance Regulatory Medical Devices Various
*Affirmative Action & OFCCP Compliance – Essentials of a Successful Plan Human Resources All Various
*The Abbreviated NDA (ANDA), 505(b)(2) Applications and Patent and Exclusivity Issues Legal Pharmaceuticals Various
*Making the Switch to Risk-based Monitoring – the Final FDA Guidance Clinical Pharmaceuticals Various
*A Practical Approach to Using Analysis of Variance (ANOVA) Quality Medical Devices Various
*Affirmative Action & OFCCP Compliance – Essentials of a Successful Plan Part II Human Resources All Various
*Writing an IFU that Meets the Needs of Patients, End Users and Regulators Labeling/Packaging Medical Devices Various
*Caring for the Uninsured in a Post-ACA World Legal Healthcare Various
*Developing Strategic Leadership – Unlocking Your Leadership Potential in Your Organization Training/Learning & Development All Various
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