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
Biosimilars Analytical Characterization and Comparability Studies
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Design for Safety
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Pharmaceutical Dissolution Testing
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Understanding and Implementing the Medical Device Directive
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The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities
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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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Food Marketing Claims: Risks of Enforcement Actions and Class Action Lawsuits, Defense Strategies and Best Practices
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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 Control Essentials for Medical Devices
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Regulatory Change and Effective Policy Management
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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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Healthcare Medical Software/Applications - Risks, Validation & Interoperability
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Medical Device Recall Management
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In Depth EU Medical Device Regulation (MDR) 2017/745 Training
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Why is FDA at my facility, and what do I do during an inspection?
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