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
Internal Audits and Supplier Audits for Life Science Companies
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Quality System Regulations for Drugs, Devices, and Tablets and How to generate your DMF
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Good Laboratory Practice (GLP) for Non-Clinical Laboratory Studies - Application and Compliance to Ensure Safety of Biologic Therapeutics and Medical Devices
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Risk Based Internal Auditing (RBIA)
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Risk Based Internal Auditing (RBIA)
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Governance, Risk Management and Compliance (GRC) for Safe and Effective Cloud Computing - Cloud Service Level Agreements (SLAs)
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Compliance in the Cloud: Maintaining Control When Moving to Cloud-Based Hosting
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OSHA General Industry
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ComplianceOnline and Risk Luminosity Seminar present 2 days Interactive Seminar:
Thriving on Risk - Risk Management for 21st Century
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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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How to Format Succinct and Comprehensive 510(k)s and PMAs
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Business Continuity and Scenario Planning
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Business Continuity and Scenario Planning
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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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