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
Project Management for Banks and Financial Institutions
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Best in Class Wage & Hour Compliance: The Federal Labor Standards Act (FLSA)
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The CMS Hospital Conditions of Participation (CoPs) Made Easy 2018
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Unannounced FDA Inspections 2017-2018: Navigating Cultural Differences
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Supplier Quality Agreements - Essential for suppliers of most outsourced processes
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Fostering Employee Engagement
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Incident Management and Crisis Prevention for Food and Consumer Goods Companies
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Applications of Statistics to Pharmaceutical Operations with Explanatory Statistics and Sampling Software
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Vendor and Supplier Qualification Program for FDA Regulated Industries
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The ISO 13485 Quality Management System | Day 2
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Good Documentation Practice and Record Keeping Regulations (FDA & EMA)
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21 CFR Part 820 Quality System Regulation and FDA cGMP Requirements for Medical Devices
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FDA Regulations for Dietary Supplements Manufacturers (21 CFR Part 111, GMP and QMS)
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Compliance in Medical Device Reprocessing - Improving Patient Safety and Department Performance
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Business Continuity Auditing Plans Using ISO 22301
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Confined Spaces in Construction. Silica in Construction
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Confined Spaces for General Industry. Lockout/Tagout
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Managing Your FDA Inspection: Before, During and After
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Biostatistics for the Non-Statistician
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Biostatistics for the Non-Statistician
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