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
Principles and Application of Hazard Analysis Critical Control Point (HACCP)
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Principles and Application of Hazard Analysis Critical Control Point (HACCP)
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FDA's Regulation of Regenerative Medicine including Stem Cell Treatments, Tissue Engineering and Gene Therapies
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Data Integrity, Good Documentation Practices and Electronic Data Governance
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A Risk Based Scientific Approach to Analytical Methods Development and Validation Activities for FDA Regulated Industries
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Managing Your FDA Inspection: Before, During and After
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Risk-based Auditing for Reserves Management Operations
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NIR Spectroscopy in the Life Science Industries (Pharma and BioPharma)
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Project Management in Accounting
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Forensic Auditing
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Good Pharmacovigilance Practices in day-to-day Pharmacovigilance
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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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