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Customized Onsite
DIA is recognized throughout the life sciences community as the definitive source for knowledge and content. That’s why top companies around the world trust DIA to deliver current, relevant, and effective education and professional Customized Onsite Training.
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Adaptive Design in Clinical Trials: When and How to Apply
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Advanced GCP Study Monitoring
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Advanced Signal Management - Detection, Evaluation, and Decision-Making
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Art of Writing a Clinical Overview
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Benefit-Risk Assessment and Management Across the Lifecycle
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Change Management, Issues Management, and Escalation Management
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Clinical Project Management
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Clinical Statistics for Nonstatisticians
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Developing Standard Operating Procedures
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Development of a Clinical Study Report
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Drug Safety and Pharmacovigilance Across the Product Lifecycle
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Electronic Submissions: The Next Era of Electronic Submissions
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Enterprise Resource Management
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Essentials of Project Management
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Essentials of Safety Medical Writing
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EU Regulation of In-Vitro Diagnostics
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European Regulatory Affairs: Keeping Your Finger on the Pulse of Marketing Authorizations
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Fundamentals of Clinical Research Monitoring
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Fundamentals of Project Management for the Nonproject Manager
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Global Regulatory Strategy and Drug Development in Asia-Pacific, Latin America and Other Emerging Markets
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Good Clinical Practices for the Clinical Research Professional
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High Performance Biopharm Teams
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How to Prepare for a Safety Inspection
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Innovative Statistical Approaches for Clinical Trials
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Introduction to Computer Systems Validation
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Introduction to Portfolio Management and Performance Metrics
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Introduction to Signal Detection and Data Mining
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Medical Affairs Training
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Medical Devices: Regulation and Lifecycle Management
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Medical Writing of Periodic Safety Update Reports (PSUR/PBRER)
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Navigating Chemistry, Manufacturing and Controls through the Drug Development Process
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New Drug Product Development and Lifecycle Management
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Oversight of Clinical Monitoring: Trends and Strategies
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Overview of Drug Development
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Overview of Drug Development in Japan
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Premarketing Clinical Safety and Pharmacovigilance
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Preparing for a US FDA Advisory Committee Meeting
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Project Risk Management
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Proven Strategies for Creating an Effective Clinical Research Program
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Regulatory Affairs for Biologics
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Regulatory Affairs: The IND, NDA, and Post-Marketing
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Safety Risk Communication for Medical Products
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Safety Risk Management: A Focus on EU RMPs and US REMS
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Signal Management in Pharmacovigilance
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Strategies for Good Clinical Practice Audits
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The Pharmacovigilance Quality Management System
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