Global Certificate in Pharma Research: Ethical Practices

• Introduction to Pharma Research Ethics: Understanding the importance of ethical practices in pharmaceutical research, including historical context and current regulations.
• Informed Consent: The process of obtaining informed consent from research participants, including legal requirements and best practices.
• Data Management and Integrity: Ensuring the accuracy, completeness, and security of research data, including data collection, analysis, and storage.
• Conflict of Interest: Identifying and managing conflicts of interest in pharmaceutical research, including financial disclosures and institutional policies.
• Clinical Trial Design and Conduct: Ethical considerations in the design and conduct of clinical trials, including participant safety, study power, and data reporting.
• Publication and Dissemination of Research Findings: Ethical considerations in the publication and dissemination of research findings, including authorship, peer review, and data sharing.
• Pharma Industry Ethics: Ethical considerations in the pharmaceutical industry, including marketing practices, pricing, and access to medicines.
• Regulatory Compliance: Understanding and complying with regulatory requirements for pharmaceutical research, including good clinical practice (GCP) guidelines and institutional review board (IRB) approval.
• Research Misconduct: Identifying and addressing research misconduct, including fabrication, falsification, and plagiarism.