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
Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)?
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Key GMP Systems in Pharmaceutical and Biotech Labs
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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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How to apply ISO 62304 standard in a medical software development project?
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Applying ISO14971 / IEC62304 / IEC62366-1 - A Practical Guide On How To Implement Risk Management
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Human Error Reduction Program: How to investigate, predict, prevent, correct & recover from Human Error in the manufacturing floor and GMP environments
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Statistical Process and Quality Control
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Developing an Effective Set of Service Level Agreements (SLAs) to Improve Quality of Service (QoS) for IT and Any Service
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Packaging and Labeling in Pharmaceutical Production
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Clinical Data Management (FDA E6 GCP Guidelines)
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Identify and Manage Data Integrity Issues, CSV and 21 CFR Part 11
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Aseptic Processing Overview and Validation
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Developing an Effective Set of Service Level Agreements (SLAs) to Improve Quality of Service (QoS)
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Contamination-Control and Cleaning and Disinfection
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