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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

 

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U.S. Human Food and Animal Feed Law- Issues Related to Food Safety, Formulation, Ingredients, Manufacturing, Labeling, Exporting and the Sale of Products in the United States
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HIPAA Omnibus Rule Compliance- Understanding Roles and Responsibilities of Privacy and Security Officers
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How to prepare a 510(k) Notification and a Technical File for the CE Mark
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Latin America - Understanding Regulatory Compliance Requirements Across The Life Science Industry
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Effective Complaint Handling, Medical Device Reporting and Recalls and Avoiding Costly Errors
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Understanding FDA QSR for Med Devices and Laser Product Performance Standards for Medical and Industrial Radiation Emitting Devices
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Medical Device Architecture - Design for Safety
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How To Build A World Class Environmental, Health & Safety Management System
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Design History Files, Device Master Records and Quality Management System for Medical Device Company - Principles of Lean Documents and Lean Configuration
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Regulatory, Technical and Partnership Management Challenges in the Co-development of Drugs and Diagnostics
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The OSHA Compliance 10 Hour Workshop
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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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ComplianceOnline and Risk Luminosity Seminar present 2 days Interactive Seminar:
Thriving on Risk - Risk Management for 21st Century
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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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How to Format Succinct and Comprehensive 510(k)s and PMAs
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