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This book looks specifically at clinical trials - those research studies that involve the active participation of people to test the safety and effectiveness of new medical treatments. The majority of clinical trials are sponsored by pharmaceutical, biotechnology and medical device companies. The purpose of the book is to present facts, information and case examples in order for you to make an informed decision about participating in a trial. What should you expect? What kinds of questions should you ask? How can you minimize your risk? The book begins with a brief history about the industry, a discussion of the drug development process and what is involved in bringing a new drug to market. What are your rights as a study volunteer? What is informed consent and what are specific federal regulations and guidelines that protect your safety and ethical treatment? Next the book describes the process of participating in a clinical trial. How do you volunteer for a study? How can you identify the appropriate trials for your condition or that of a family member or friend? The book also contains ideas and impressions from people who have actually participated in clinical trials.

geïnformeerde vrijwillige toestemming (instemming) --- klinische proef (klinische studie, geneesmiddelenstudie) --- Verenigde Staten --- consentement libre et éclairé --- essai clinique (étude clinique) --- Etats Unis --- Clinical trials. --- Informed consent (Medical law) --- Consumer education. --- Clinical Trials. --- Informed Consent. --- Patient Acceptance of Health Care.