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
Understanding and Implementing the New ICH/USP Elemental Impurity Guidelines
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Preparing for and Managing Health Authority Inspections (FDA/EMA/TGA)
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Transferring A Medical OEM Molding or Assembly Operation to A World Class Contract Manufacturer With FULL Validated Systems And Processes
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US GCP Fundamentals for Pharmaceutical and Biologic Companies
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The Complete Payroll Law Seminar - Red flags, Most Recent Case Studies affecting Payroll, Overtime Pay, Comp Time, the FMLA, the ACA and Many More
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Product Information for Medicinal Products in the EU
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Root Cause Analysis and CAPA using 8-D Problem Solving Method
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Strategic Human Resources Management Program for HR Professionals
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Auditing for Medical Device and Pharma Companies – A Tool to Reduce Quality and Compliance Risk
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Lifecycle Management of Analytical Methods and Procedures - Integrate design, development, validation, and ongoing performance verification according to new FDA and USP guidelines
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Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products
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Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products
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World Class Risk Management - What The Best International Standards Say About Risk - ISO 31000, ISO 14971 and ICH Q9
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World Class Risk Management - What The Best International Standards Say About Risk - ISO 31000, ISO 14971 and ICH Q9
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Analyze Safety In The Workplace: Inspections, Management Techniques & Training Methods
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Recognizing and Investigating Payments Fraud
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World Class Risk Management - What The Best International Standards Say About Risk - ISO 31000, ISO 14971 and ICH Q9
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Biopharmaceutical Test Method, Methods from Cradle to Grave - Technical, Regulatory & Business Considerations
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Bioanalytical Methods and Good Laboratory Practices (GLP) - Essential Elements for Pre-Clinical Studies during development of Drugs
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Operation's Risk Management - A Practical Approach (ISO 31000:2009 Guidelines)
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