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
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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Risk Management and Post Market Surveillance for Medical Devices: Developing a Better Living Knowledge Base to Improve it
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Design for Safety
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Pharmaceutical Dissolution Testing
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Regulatory Change and Effective Policy Management
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Healthcare Medical Software/Applications - Risks, Validation & Interoperability
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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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Why is FDA at my facility, and what do I do during an inspection?
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Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency
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Design Control Essentials for Medical Devices
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Understanding FDA and Avoiding Inspections Leading to Warning Letters, Seizures, Injunctions and Prosecutions
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Fighting Corruption - the FCPA, Anti-Bribery Act, and OECD compliance
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Good Corporate Governance
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