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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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Quality by Design: A New Paradigm for the Development and Commercialization of Biopharmaceuticals
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Investigational New Drug (IND) & Investigational Device Exemptions (IDE) Applications Preparation and Submission, and Conducting FDA Meetings
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Corrective and Preventative Action Topics: Investigation Phase, Action Phase and Verification of Effectiveness Phase
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Pharmaceutical Analysis for Small Molecules and Regulatory Requirements
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Pharmacovigilance of Drugs, Vaccines & Devices - Recent FDA Regulations and Technology Updates
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The Internal Audit Process Ethics and the Internal Auditor
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A Practical Hands-on Approach to Conducting Quantitative Analysis
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How to Start a Healthcare Compliance Program
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Coding Evaluation and Management (E/M) From a Physician's Perspective
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Risk Management System in Medical Devices Industry
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Risk Management System in Medical Devices Industry
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Healthcare Privacy and Security Regulations: Satisfying HIPAA, GDPR, 42 CFR Part 2, FERPA, and State Laws Protecting Health Information
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Is your Medical Device Software 510(k) Ready?
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Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results
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Process Enhancement through Quality by Design (QbD)
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Optimizing Dissolution Method Development for Different Types of Products and Evaluating the Data
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Project Management in Clinical Research
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Food Safety and Defense: Key Factors to Safely Manufacture, Package and Handle Food Products
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Social Media Crisis Management
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New Hazard Communication & Global Harmonized System, and OSHA Record Keeping
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