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
How to Prepare for an FDA Meeting: Making the Most of Pre-IND/IDE, pre-NDA and Other Critical Meetings
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GMP Compliance for Quality Control and Contract Laboratories
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Analytical Instrument Qualification and System Validation
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Managing an Effective AML Compliance Program
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Conducting Effective Investigation of Out-of-Specs and Atypical Laboratory Data
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Drug Law: Understanding the Essentials of FDA's Authority over Innovative and Generic Pharmaceuticals
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The Sunshine Act--Are You Prepared? The March 31 Reporting Deadline is Roughly 5-Months Away!
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6 Hr Virtual Seminar on FinTech for Non-IT Professionals
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Understanding and Implementing the Medical Device Directive
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Root Cause and Root Cause Analysis and Out-Of-Specification (OOS) Training
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Bulletproof CAPA Handling and Investigations for Medical Devices
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Detecting and Preventing Health Care Fraud and Ethics for Fraud Deterrence
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Manufacturing and Marketing OTC Drugs in Compliance with FDA Regulations (Updated to address recent Homeopathic Drug announcements by FDA & FTC)
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Changes to the 510(k) System - Impact on Innovation, Investment, and Business Development
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Managing Employee Leaves, Health Issues, Disability and Job Accommodation: A Practical Guide to the ADA, FMLA, Workers' Compensation, and Military Leave
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The European Clinical Trial Directive…Plus…European Filings and Registration Procedures
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Medical Device Quality Systems, Quality System Regulations, and CAPA
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Introduction to Risk Management and Business Process Mapping Skills
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Effective Risk Management Strategies for the Department and the Enterprise
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Effective Risk Management Strategies for the Department and the Enterprise
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