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
Clinical Data Management (CDM)
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Business Continuity Auditing Plans Using ISO 22301
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Business Continuity Auditing Plans Using ISO 22301
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REACH and RoHS Compliance: Gain a Deeper Understanding
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REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance
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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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The Medical Device Directive | Day 3
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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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Principles and Application of Hazard Analysis Critical Control Point (HACCP)
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FDA's Regulation of Regenerative Medicine including Stem Cell Treatments, Tissue Engineering and Gene Therapies
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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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Managing Your FDA Inspection: Before, During and After
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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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