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
Fostering Employee Engagement
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Incident Management and Crisis Prevention for Food and Consumer Goods Companies
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Applications of Statistics to Pharmaceutical Operations with Explanatory Statistics and Sampling Software
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Vendor and Supplier Qualification Program for FDA Regulated Industries
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New Hazard Communication & Global Harmonized System, and OSHA Record Keeping
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Key GMP Systems in Pharmaceutical and Biotech Labs
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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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Managing Your FDA Inspection: Before, During and After
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Clinical Data Management (CDM)
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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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Developing an Effective Set of Service Level Agreements (SLAs) to Improve Quality of Service (QoS) for IT and Any Service
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Biocompatibility Testing for Medical Devices
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