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
Analytical Methods in Development and Manufacture of Drugs and Biologics
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How to Preventing Root Cause and Conduct Analysis for Corrective Action after an Incident or Non-conformance
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Analytical Methods in Development and Manufacture of Drugs and Biologics
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Essential Skills Crash Course for the HR Professional
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Focus Four Construction: Top 4 Life Critical Safety Issues to Avoid
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Harmonized Tariff Schedule and Schedule B
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Global Medical Device Regulations - US, EU, Canada, Argentina, Australia, Brazil, India, Japan, Mexico, Russia, South Korea, Taiwan
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Mastering Risk Based Internal Auditing (RBIA)
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Analytical Methods in Development and Manufacture of Drugs and Biologics
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21 CFR Part 11/Annex 11 compliance for software validation and SaaS
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SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations
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6 Hr Virtual Seminar on Risk Based Internal Auditing “RBIA”
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Strategic Supply Stream - Developing perspective- C-TPAT, ISA, Trusted Trader SRM/SSRM
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Keeping Secrets beyond HIPAA: How to Maintain and Dispose of Patient Medical Records and Keep Client Confidentiality in Mental Health
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FDA's Regulation of Implantable and Wearable Sensors
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How to Perform a Cognitive Load Assessment for Human Error Reduction
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Advertising and Promotion of Dietary Supplements
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Meeting ILAC Requirements for Measurement Traceability to the SI through NIST and other National Metrology Institutes
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Managing Risk in Electronic Banking - A 2-day intensive course on Risk Management & Mitigation in eBanking Activities
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Data Integrity: FDA/EU Requirements and Implementation
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