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
Robust Quality System Approach to Pharmaceutical Products: Scientific Basis and Implementation of Current Regulations
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Recordkeeping and Documentation in a GLP Laboratory (US FDA, US EPA and OSHA Focus)
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Writing and implementing a Standard Operating Procedure (SOP) in a Compliant Laboratory (US FDA, US EPA and OSHA Focus)
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AML/CTF Investigation and Identification
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Implementing the New Australian Standard for Product Recall
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How to Pass the Customs Broker Exam?
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A risk based approach to GxP Compliant Laboratory Computerized Systems
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Biostatistics for Non-Statisticians in Pharma and Medtech
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FDA's New Import Program for 2018 - Strict Precision
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FDA's Medical Device Software Regulation Strategy
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International Trade Finance
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How to Navigate and Manage Employee Leave Issues under the FMLA, ADA and Workers' Comp Laws
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New Hazard Communication & Global Harmonized System, and OSHA Record Keeping
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Unconscious Bias: Minimizing Impact on Discrimination, Hiring, Promotions, & Retention
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Labelling and Presentation of Food Products in the European Union
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Operations Risk - Active Management Across Industries
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World Class Cyber Incident Response Plans: Strong Responses to Attacks
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Bad Things Happen, But It Can Get Worse - Understanding FDA Post Market Regulations
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FDA Penalties for Non-Compliance in Pharma - 2017 case studies and Readiness for 2018
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Project Management for Banks and Financial Institutions
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