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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

 

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Regulated Laboratory Inspections - Be Prepared, Be Validated and Avoid Observations
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Effectively Addressing and Remediating FDA's Form 483 Findings, Warning Letters and Consent Decree Compliance Issues
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Compliant Clinical Research Conduct: What Every Clinical Research Professional Needs to Know
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Good Corporate Governance
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International Payments - Advanced Workshop
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Overview of clinical drug development from final preclinical selection, marketing approval, all phases of clinical trials, new strategies, challenges and solutions
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The A to Z's of Microbial Control, Monitoring and Validation of Water Systems for Pharmaceuticals, Biologics, Medical Devices, Cosmetics, and Personal Care Products
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Human Resources and Employment Law Essentials
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Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
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MetricStream Roundtable: Meet CEO of MetricStream (#2 Most Influential African American in Technology)
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Validation and Part 11 Compliance of Computer Systems and Data
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FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials

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ComplianceOnline Pharma Summit 2016 - Risk Control and Compliance
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Accounting and Bookkeeping Best Practices
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Project Management in Human Resources
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The Job of the Corporate Controller in Today's Environment
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Effective Financial Compliance: How to Defend SEC and Financial Regulatory Enforcement Actions and Examinations
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CDISC Mapping and Strategies Implemented
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Design of Experiments (DOE) for Process and Product Optimization
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