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
Risk Management System in Medical Devices Industry
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Risk Management System in Medical Devices Industry
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Healthcare Privacy and Security Regulations: Satisfying HIPAA, GDPR, 42 CFR Part 2, FERPA, and State Laws Protecting Health Information
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Is your Medical Device Software 510(k) Ready?
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Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results
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Process Enhancement through Quality by Design (QbD)
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Optimizing Dissolution Method Development for Different Types of Products and Evaluating the Data
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Project Management in Clinical Research
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Food Safety and Defense: Key Factors to Safely Manufacture, Package and Handle Food Products
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Social Media Crisis Management
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Developing an Effective Set of Service Level Agreements (SLAs) to Improve Quality of Service (QoS)
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Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)?
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Contamination-Control and Cleaning and Disinfection
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Basel III, IV and Beyond - Effective Risk Data Management and Reporting
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Negotiating the Labor Agreement
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Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)?
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How to Implement a Quality Management System According ISO 13485?
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How to apply ISO 62304 standard in a medical software development project?
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International Trade Finance
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How to Implement a Quality Management System According ISO 13485?
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