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
HRM and the High Performance Organization
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Managing Regulatory Inspections Training - The Dos and Don'ts Before, During And After an FDA GCP Inspection
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Business Continuity & Scenario Planning
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Navigating Federal Wage and Hour Compliance Issues under the Fair Labor Standards Act
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Clinical Trial Essentials; Implementation Best Practice
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Facility, Maintenance and Calibration Considerations of the Quality Systems Inspection Technique (QSIT)
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Fundamentals of EU MDR and IVDR – Level 1
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Introduction into the EU IVDR 2017/746 - the new EU regulation for invitro diagnostic medical devices
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Financial Life Cycle of Clinical Research Studies: Best Practice Approaches
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Medical Device Seminar Series: QSR, Design Control and Pre-Market Submissions
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Design for Safety
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Pharmaceutical Dissolution Testing
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Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations
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Risk Management Challenges and Solutions: A Practical, Cost-Effective, Hands-On Approach to Implementing Risk and Internal Controls from a Management Perspective
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Transforming Corporate Spending Processes: T&E and AP Best Practices and Digitization
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European Union Regulatory Issues - Product Development for Solid Oral Dosage Forms
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Comprehensive Seminar on Everything You'd Like to Know about Pharmaceutical Water Systems, But were Afraid to Ask
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Pharmacovigilance System Master File (PSMF) - A Practical Approach to Design and Implementation Globally
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Equipment and Utilities Qualification
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Biosimilars Analytical Characterization and Comparability Studies
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