Robinson / Cook Clinical Trials Risk Management

Erscheinungsjahr 2005
ISBN: 978-1-4200-3765-4
Verlag: Taylor & Francis
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

E-Book, Englisch, 232 Seiten

Drug development is risky business. It is against the backdrop of huge financial, scientific, technical and medical risks that a clinical trials manager is expected to function, effectively identifying and managing all project risks, to deliver a successful outcome. Focusing on the day-to-day needs of a clinical trials manager, Clinical Trials Risk Management explains the key concepts and principles of risk management, as well as showing how best to how to apply them directly to 'real life' clinical trial situations.

After building a foundation of basic principles, the authors lead you through specific methods for handling the risks characteristically encountered in clinical trials. Their combined years of experience in pharmaceutical research and development shine through the narrative, making the prose both lively and informative. They discuss concepts using worked examples and include a summary of the main points at the end of each chapter. In addition to diagrams and Risk and Precision Tree charts, the text is sprinkled with humorous line drawings that reinforce the concepts.

After reading this book, you will know how to:
- Prepare a Risk Assessment

- Design an Impact-Probability Matrix

- Compile a Risk Register

- Run a Monte Carlo Simulation

- Set up a Project Decision Tree

- Plan preventative and contingency actions

The stand-alone chapters provide easy access to topics, while anecdotal and visual examples make them easy to remember. Martin Robinson and Simon Cook deliver a clear interpretation of complex information, thus saving you the time it would take to wade through a lengthier text, adopting a straightforward approach to examining clinical trials from a risk manager's perspective. A practical, readable guide, the book is filled with information that can be put to immediate use to improve current or planned clinical trials.

Zielgruppe

Clinical trial principle investigators and project managers and other clinical research professionals, project team leaders/pharmaceutical scientists developing new drugs, and FDA regulatory personnel

Autoren/Hrsg.

Robinson, Martin

Cook, Simon

Fachgebiete

• Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Medizinische Fachgebiete Pharmakologie, Toxikologie

Inhaltsverzeichnis

DEFINITIONS AND CONCEPTS
What is Risk?
The Principles of Risk Management
Drug R&D: A Risky Business
Why Risk Management in Important in Clinical Trials

DRUG SAFETY AND PHARMACOVIGILANCE
USA
Japan
European Union

TYPES OF RISK IN CLINICAL TRIALS
The Life Cycle of a Clinical Trial
Typical Risks that Clinical Trial Projects Face
Internal and External Risks

RISK IDENTIFICATION
Brainstorming a Risk Assessment
Compiling a Risk Register
Assessing Impact and Probability
Simulation Models

THREATS AND OPPORTUNITIES
Responding to Threats
Maximizing Opportunities
Stakeholder Needs and Risk Tolerance

PLANNING PREVENTATIVE STRATEGIES
Assessing Cause
Creating s Prevention Plan
Controlling the Critical Path

BACKUP PLANNING
Contingency Planning
Trigger Points

TRACKING RISKS
Detecting Symptoms
Responding to Deviations
Continuous Risk Management
Decision Milestones

INVESTIGATIONAL SITE RISK MANAGEMENT
The Role of the CRA in Individual Site Risk Assessment
Initial Risk Analysis Before and During the Prestudy Visit
Using the Initiation Visit for Risk Prevention
Ongoing Risk Management through Monitoring

POST PROJECTION EVALUATION
Reviewing Success of Risk Management Strategy
Learning Lessons for the Future