Chapter 1. The Roadmap to Research: Fundamentals of a Multifaceted Research Process.- Chapter 2. Processes involved in the generation of novel ideas.- Chapter 3. Creativity and critical thinking contribute to scholarly achievement.- Chapter 4. Writing protocols in Pharmacological studies.
- Chapter 5. Basics of Designing General Toxicology Studies.- Chapter 6. General design considerations in Reproductive and developmental toxicity studies.- Chapter 7. Genetic toxicology studies.- Chapter 8. Rodent Carcinogenicity Studies.
-Chapter 9. Designing studies in pharmaceutical and medicinal chemistry.- Chapter 10. Experimental protocols in phytochemistry and natural products: an ever-evolving challenge.- Chapter 11. Drug substance/ product quality analysis (Quality assessment).- Chapter 12. Drug Delivery Systems: Lipid Nanoparticles Technology in Clinic.
- Chapter 13. Pharmacokinetic studies for drug development.- Chapter 14. New Alternative Methods in drug safety assessment.- Chapter 15. Animal models for the study of human disease.- Chapter 16. Physiologically based Pharmacokinetic Modelling in Drug Discovery and Clinical Development: A Treatise on Concepts, Model Workflow, Credibility, Application and Regulatory Landscape.
- Chapter 17. Design and conduct of pharmacokinetics studies influenced by extrinsic factors.- Chapter 18. Specific Populations: Clinical Pharmacology Considerations.- Chapter 19. Impact of genetic variation on drug response.-Chapter 20. Phases of clinical trials.
- Chapter 21. Common clinical trial designs.- Chapter 22. Elements of clinical trial protocol design.- Chapter 23. Good clinical practice in clinical trials, substantial evidence of efficacy, and interpretation of the evidence.- chapter 24. Grandfathered Drugs of 1938 in the United States.
- Chapter 25. General overview of the statistical issues in clinical studydesigns.- Chapter 26. Introduction to pharmacoepidemiology and its application in clinical research.- Chapter 27. Pharmacovigilance through phased clinical trials, post-marketing surveillance and ongoing life cycle safety.- Chapter 28. The design and statistical analysis of randomized pre-clinical experiments.
- Chapter 29. Descriptive and Inferential Statistics in Biomedical Sciences: an overview.- Chapter 30. Principles and applications of statistics in biomedical research: parametric and non-parametric tests including tests employed for Post-hoc analysis.- Chapter 31. Artificial intelligence generative chemistry design of target-specific scaffold-focused small molecule drug libraries.- Chapter 32. Artificial intelligence technologies for clinical data pharmacoanalytics.
Case studies on Alzheimer''s disease.- Chapter 33. Bioinformatics: Theory and Application.- Chapter 34. Drug targets and drug discovery research.- Chapter 35. Role of Nonclinical Programs in Drug Development.- Chapter 36.
Drug repurposing: strategies and study design in bringing back old drugs to the mainline.- Chapter 37. Empowering knowledge on efficient literature search: an overview of biomedical search engines and databases.- Chapter 38. Literature Reviews: An Overview of Systematic, Integrated, and Scoping Review.- Chapter 39. How To Create A Bibliography.- Chapter 40.
Publication metrics /Bibliometrics.- Chapter 41. How to write a scientific paper.- Chapter 42. Preparing and structuring a manuscript for publication.- Chapter 43. Writing a scientific article.- Chapter 44.
How to Present Results in a Research Paper.- Chapter 45. Communicating results of quantitative research.- Chapter 46. How to Efficiently Write a Persuasive Discussion Section.- Chapter 47. Submitting a manuscript for publication, the peer review process, and getting past the gatekeepers.- Chapter 48.
Writing a Postgraduate or Doctoral Thesis: A Step-by-Step Approach.- Chapter 49. Poster presentation at scientific meetings .- Chapter 50. Strategies for the preparation and delivery of oral presentation.- Chapter.-51. Grant Process and Peer Review US National Institutes of Health System.
- Chapter 52. Rigor and specifics in writing research proposal.- Chapter 53. Writing research grant proposals from an Indian Perspective.- Chapter 54. Funding opportunities (resources) in biomedical sciences: Indian perspective.- Chapter 55. Mentorship in biomedical sciences.
- chapter 56. Commercializing the technology - transitioning from the academic lab to the market.- Chapter 57. Patent law fundamentals for biomedical scientists.- Chapter 58. Research integrity: responsible conduct of research.- Chapter 59. Publication integrity, authorship, and misconduct.