A Comprehensive Clinical Research Manual

Book Summary of A Comprehensive Clinical Research Manual Table of Contents Evolution of the Homo Sapiens and his Mutant, the Clinical Investigatoriens Clinical Research: Dotted, Spotted, Colored and Flavored The Protocol: "Thou Shalt Pay Thy Obedience" The Case Report Form (CRF): Hardcore Proof of Your Work Obtaining Informed Consent: Essentially a Ritual or an Essential Ritual That Magical Phrase: GCPs (Good Clinical Practices) Use of Surrogate Markers in Clinical Research: Haste that does not Waste Facts and Figures: Fodder for the Statistician Parametric and Nonparametric Tests Be Wholesome and Avoid Criticism Later Interpreting Statistical Jargon: Clarifying Obscurity Data (Handling): Not Fragile and Breakable but Handle with Care Portfolio and Project Management: Intellectual Property: Types, Rights and Caveats Ethics of Clinical Research: Think Just and Act Just Conflicts of Interest: Transparency may Invoke Evidence-Based Medicine (EBM): Need of the Day Scientific misconduct: Plain carelessness or....? Appendix I. Table of Contents of a Protocol Appendix II. Random Number Table Appendix III. Sample Case Record Form (CRF) for a Small, Nonfounded, Investigator Initiated Diabetes Study Appendix IV. Informed Consent Document Template Appendix V. Nomogram for Sample Size Calculation Appendix VI. The Declaration of Helsinki Appendix VII. The Nur

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