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
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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Navigating the Japan and South Korean Regulatory Compliance and Clinical Trial Environment
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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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CA&PA for Medical Devices
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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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Auditing the Human Resource Function
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Effective Audit Report Writing
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Application of Disinfectants and Sterilants to Control Microorganisms; FDA Endotoxin Test - Understanding the Latest Revision
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California Laws Regulating Employment Screening and Safe Hiring
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Project Management in Human Resources
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Anti-Corruption Compliance - Understanding the OECD Anti-Bribery Convention, the US' Foreign Corrupt Practices Act (FCPA), and the UK Anti-Bribery Act: A Practical Hands-On Intensive
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Fighting Corruption and Unethical Practices
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How to Successfully Manage an FDA High Risk Food Inspection
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APT Audit Process - How Agile is Your Audit Process? Risk Based Auditing 2020
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U.S. B2B Payments: The Environment, the Players, and the Regulatory and Compliance Issues It Must Endure
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How to Adequately Prepare your Company to do Business with the Government and Win Government Contracts
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