SEMINARS
Upcoming In-person and Virtual Seminars by Ex-FDA and other regulatory experts.
Get Trained on - FDA Audits and Inspections, FDA’s GMP Expectations, Clinical Trials, Vendor Selection, FDA’s New Import Program, FDA Recalls, CAPA and more
Enterprise Risk Management
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Annual Risk Assessment (ARA): Focus on Enterprise Risk Management (ERM) and Fraud Risk Assessment (FRA)
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Managing Risk through PHI Mapping: Do You Know Where Your Data Is
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Building Your Business Internationally: How to successfully import and export
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Fundamentals of Antitrust and Competition Law: What you need to know to identify issues, mitigate risk and maximize flexibility
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5th Annual ComplianceOnline Medical Device Summit 2020
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Quality Management, GMP and Regulations - Impact on Food, Seafood and Nutritional Supplements
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Conflict Minerals 2014: Looking Back and Looking Ahead
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Applying the FDA Food Safety Modernization Act (FSMA) to Your Organization
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Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices
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Lifecycle Approach to Analytical Methods for Drug Products: Incorporating QbD Concepts into Method Development, Validation, Verification and Transfer
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Technical and Regulatory Writing for FDA Regulated Industries
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CA&PA for Medical Devices
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Reducing Taxes and Managing Accounting for Efficient Business Investments
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Roadmap to Advanced Human Resources and Employment Law Essentials
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Auditing the Human Resource Function
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FDA's Medical Device Software Regulation Strategy
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TurboEIRs and their Use within Warning Letters to Illustrate the FDA and Health Canada CFRs
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Human Resource Metrics | Day 2
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Effective Audit Report Writing
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