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
Life Sciences Risk Management A to Z - Best Practices for Effectiveness and Efficiency
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Developing Documents and Records to meet ISO 17025 Requirements
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Data Integrity: FDA/EU Requirements and Implementation
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Best Practices for Safety Reporting in Clinical Trials for Drugs, Biologics and Medical Devices
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Cyber Security Incident Response Program (CSIRT) and Plans
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Aerospace Program Management - It's More than Scheduling and Delivery
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How to Minimize FCPA Exposure and Conduct Comprehensive Internal Investigations
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Canada Documentation and Procedures
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ComplianceOnline Banking Summit 2017 | Risk Management and Data Security
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FDA Scrutiny of Purchasing/Supplier Controls
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Designing a Supplier Qualification Program
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Data Integrity in Pharmaceutical and Biotech Labs
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Implementing an Effective Operational Risk Management Program
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Building a Fair and Equitable Pay Program
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eCTD Submissions of IND and NDA/BLA to the US FDA
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Data Integrity: FDA, WHO and EMA's Requirements
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The Benefit/Risk Ratio: Pharmacovigilance, Medical And Regulatory Converge
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Implementing an Effective Regulatory and Policy Change Management Process
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Creating Reader-Focused Technical Documents in FDA Regulated Industries
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OIG Work Plans: How They Impact Providers
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