Research Articles
FDA Adverse Event Reporting in Clinical Trials: A Complete Guide for Research Professionals
This comprehensive guide details the FDA's requirements for adverse event (AE) and serious adverse event (SAE) reporting during clinical trials of drugs and biologics.
Beyond the Headlines: A Deep Dive into High-Profile Cases of Scientific Misconduct in Biomedical Research
This article provides a comprehensive analysis of scientific misconduct in the biomedical field, targeting researchers, scientists, and drug development professionals.
Ultimate Guide to Data Security for Research Labs: Protection Strategies for Sensitive R&D
This comprehensive guide empowers researchers, scientists, and drug development professionals to navigate the complex landscape of data security.
The European Code of Conduct for Research Integrity: A Complete Guide for Scientists & Drug Developers
This comprehensive guide explores the European Code of Conduct for Research Integrity (ECCRI), detailing its core principles, practical application in biomedical research, strategies for navigating common challenges, and its role...
From Principles to Practice: A Complete Guide to the EthicsGuide Six-Step Method for Clinical Guidelines
This article provides a comprehensive guide for researchers, scientists, and drug development professionals on implementing the EthicsGuide six-step method for developing clinical practice guidelines (CPGs).
Lab Data Ethics: A Complete Guide to Responsible Management for Research Integrity
This comprehensive guide establishes essential ethical frameworks for managing laboratory data.
Building a Robust Data Integrity Training Program for Researchers: A Comprehensive Framework for Scientific Excellence
This article provides a complete guide for research institutions and pharmaceutical R&D teams to establish effective data integrity training programs.
Paper vs. Electronic Lab Notebooks: A 2024 Guide to Data Integrity for Scientific Research
This comprehensive guide examines the critical choice between Paper Lab Notebooks (PLNs) and Electronic Lab Notebooks (ELNs) in the context of data integrity—a cornerstone of scientific research, regulatory compliance, and...
Beyond Compliance: Measuring What Works in Research Integrity Training for Scientific Excellence
This article provides a comprehensive analysis of research integrity training program effectiveness for biomedical researchers and drug development professionals.
Navigating Ethical, Legal, and Social Implications: A Comprehensive Guide to ELSI Study Design for Recall-by-Genotype Research
This article provides a detailed roadmap for designing robust ELSI (Ethical, Legal, and Social Implications) studies integrated within Recall-by-Genotype (RbG) research frameworks.