Clinical Research: Scientific Communication and Transfer of Results

Research Methodology · Clinical Bases

How it begins

Un análisis exhaustivo de los mecanismos moleculares de la transferencia de tecnología, la bioestadística aplicada a la publicación científica de alto impacto, la ética del reporte metodológico y la traducción del descubrimiento biofarmacéutico en patentes y propiedad intelectual.

What it covers

1. Communication and Transfer
2. Ethics and History of Scientific Communication
3. · The Evolution of Scientific Communication
4. · Ethical Foundations of Disclosure
5. Scientific Article Structure (IMRaD)
6. · Advanced Statistical Analysis in the Methods Section
7. · Intention to Treat (ITT) vs. By Protocol (PP)
8. Scientific Writing and Reporting Guidelines
9. · Patient Flow Structure according to CONSORT
10. Selection of Journals and Bibliometric Metrics
11. · Main Scientific Metrics and Their Mathematical Foundations
12. · Comparison of Global Metric Indexing Systems
13. · The Threat of Predatory Publishers
14. The Peer Review Process and Reply Letters
15. · The Response Letter to the Reviewers (Rebuttal Letter)
16. Scientific Integrity, Biases and Retractions
17. · COPE Flowchart for Action on Suspected Plagiarism
18. · Historical Cases of Scientific Fraud and their Impact
19. Intellectual Property in Clinical Research
20. · Criteria for Patentability of Medical Inventions
21. Patents vs. Scientific Publication
22. · Structure of an International Patent Application (PCT)
23. Technology Transfer Offices (OTRI/TTO) and Spin-offs
24. · Mechanisms for the Exploitation of Medical Technology
25. Open Science, Preprints and the Plan S Movement
26. · The Impact of Plan S and the Transition of Models
27. Social Scientific Dissemination and Public Communication of Results
28. · Strategies for Responsible Disclosure without "Spin"
29. Public Records of Clinical Trials
30. · Main Trial Registration Platforms
31. Communication to Regulatory Entities (FDA, EMA)
32. · The Organizational Structure of the Common Technical Document (CTD)
33. · ICH-GCP Ethical and Quality Standards
34. Impact Monitoring, Altmetrics and Disinformation