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
21 CFR Part 820 Quality System Regulation and FDA cGMP Requirements for Medical Devices
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FDA Regulations for Dietary Supplements Manufacturers (21 CFR Part 111, GMP and QMS)
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Compliance in Medical Device Reprocessing - Improving Patient Safety and Department Performance
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Business Continuity Auditing Plans Using ISO 22301
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Confined Spaces in Construction. Silica in Construction
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Confined Spaces for General Industry. Lockout/Tagout
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Contamination-Control and Cleaning and Disinfection
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REACH and RoHS Compliance: Gain a Deeper Understanding
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Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans
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FDA's New Import Program for 2018 - Strict Precision/U.S. Imports (Export from Singapore)
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HRM and the High Performance Organization
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Biocompatibility Testing for Medical Devices
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Principles and Application of Hazard Analysis Critical Control Point (HACCP)
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Data Integrity, Good Documentation Practices and Electronic Data Governance
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A Risk Based Scientific Approach to Analytical Methods Development and Validation Activities for FDA Regulated Industries
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Risk-based Auditing for Reserves Management Operations
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NIR Spectroscopy in the Life Science Industries (Pharma and BioPharma)
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Project Management in Accounting
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Forensic Auditing
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Good Pharmacovigilance Practices in day-to-day Pharmacovigilance
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