Re-Engineering Clinical Trials
Best Practices for Streamlining the Development Process
Gebonden Engels 2014 9780124202467Samenvatting
The pharmaceutical industry is currently operating under a business model that is not sustainable for the future. Given the high costs associated with drug development, there is a vital need to reform this process in order to provide safe and effective drugs while still securing a profit. Re-Engineering Clinical Trials evaluates the trends and challenges associated with the current drug development process and presents solutions that integrate the use of modern communication technologies, innovations and novel enrichment designs. This book focuses on the need to simplify drug development and offers you well-established methodologies and best practices based on real-world experiences from expert authors across industry and academia. Written for all those involved in clinical research, development and clinical trial design, this book provides a unique and valuable resource for streamlining the process, containing costs and increasing drug safety and effectiveness.
Specificaties
Lezersrecensies
Inhoudsopgave
1. Why is our industry struggling?
2. What are the current main obstacles to reach drug approval?
3. Japan: An opportunity to learn?
4. The "Clinical Trial App"
Section 2: What Does Our Industry and What Do Others Do
5. What does "re-engineering" mean in our industry?
6. How can the Innovative Medicines Initiative help to make drug development more efficient?
7. Experiences with Lean and Shopfloor Management in R&D in other branches
8. Well-known methodologies, but not in our world: FMEA
Section 3: Where to Start: The Protocol
9. No patients, no data: Patient recruitment in the 21st century
10. The impact of bad protocols
11. Data mining for better protocols
12. It is all in the literature
13. What makes a good protocol better?
14. The Clinical Trial Site
Section 4: Alternative Study Designs
15. Do we need new endpoints? Surrogate and bio-marker
16. On the measurement of the disease status in clinical trials: lessons from MS
17. Generating evidence from historical data using “robust prognostic matching: Experience from Multiple Sclerosis
18. Studies with fewer patients involved: the Adaptive Trial
19. Studies with less site involvement: the Hyper Trial
20. Studies without sites: the Virtual Trial
Section 5: From Data to Decisions
21. Data standards against data overload
22. Data management 2.0
23. What do Sites Want?
24. From data to information and decision: ICONIK
25. Knowledge Management
26. Taking Control of Ever Increasing Volumes of Unstructured Data
27. Share the Knowledge based on quality data
Section 6: You Need Processes, Systems and People
28. It's all about the people (and their competencies)
29. Manage the Change
30. How Key Performance Indicators help to manage the change
Conclusions
Rubrieken
- advisering
- algemeen management
- coaching en trainen
- communicatie en media
- economie
- financieel management
- inkoop en logistiek
- internet en social media
- it-management / ict
- juridisch
- leiderschap
- marketing
- mens en maatschappij
- non-profit
- ondernemen
- organisatiekunde
- personal finance
- personeelsmanagement
- persoonlijke effectiviteit
- projectmanagement
- psychologie
- reclame en verkoop
- strategisch management
- verandermanagement
- werk en loopbaan