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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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Production and Process Control: Building a Robust System for Medical Device Companies
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FDA Scrutiny of Promotion and Advertising Practices
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OSHA - Fall Protection
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Fostering Transparency and Accountability to Combat Money Laundering and Illicit Financial Flows (IFF) in Africa
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Process validation and process defect prevention to increase device reliability
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HAZWOPER 8 HOUR COURSE (Hazardous Waste Operations and Emergency Response): An Interactive
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Elements of Current Good Manufacturing Practices (cGMP) for Complying with the Food Safety Modernization Act (FSMA)
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The A to Z of Trade Compliance for a U.S. Entity
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Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines
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OSHA 10 Hour Course
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A Practical Approach to Managing an Anti-Money Laundering Program
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The New Clinical Trials Regulation and Regulatory Affairs Aspects of Medicinal Product Development in the EU
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Identity Theft Exposure and the Methods Utilized to Prevent and Detect the Transfer of Illegal Funds through Financial Institutions
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Forensic Accounting and Fraud Examination Exercises
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Import Procedures and Documentation
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Internal Control Best Practices for your Procure to Pay (P2P) Process
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Aseptic Processing Challenges
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Computer System Validation - Reduce Costs and Avoid 483
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FDA Compliant GLP for Nonclinical Studies - For Pharmaceutical and Medical Device Industries
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Detecting and Preventing Embezzlement in Your Organization
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