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
Building a Risk Based Internal Audit Plan: What Matters to the Organization
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Essentials of ERM and Assessing its Effectiveness Using ISO 31000
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Risk Management - Focus on Fraud
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Risk Management - Focus on Fraud
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International Trade: Strategies to Enhance Financing and Operational Success
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Operations Risk Management and Mitigation - from Assessment to Implementation
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Compliance Processes for Life Science Products in Brazil, Russia, India, China markets - Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations
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Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency
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The CE Mark: Understanding the Medical Device Directives
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The Microbiological Element of Cleaning Validation in Oral Solid Dosage Manufacturing
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Developing an Environmental Monitoring Strategy for a Non-Sterile and Aseptic Processing Area (Controlled/Classified Environment) -- To Include HVAC and Utility Systems
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CLIA Waiver and Dual 510(k) CLIA Waiver Submissions to FDA
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Navigating the Japan and South Korean Regulatory Compliance and Clinical Trial Environment
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Smart Tax and Accounting Solutions for Small Business
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Detecting and Preventing Asset Misappropriation and Financial Statement Fraud
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Schedule M-1/M-3 and Schedule UTP Reporting and Companies Requirements
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Software Risk Management - Ways to FDA and MDD Compliance
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Beyond HIPAA: Developing Your Privacy and Information Security Programs in Healthcare Organizations
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Individual Tax Minimization Strategies for 2015
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COSO Framework for Internal Controls, Risk Assessment and Financial Statement Audit
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