The author shares their extensive knowledge of clinical trials operations, research compliance and quality assurance with individuals interested in pursuing a career in providing access to clinical trials to patients as part of medical care. Well-designed and -conducted clinical trials are our best chance to develop safe and effective treatments. Building a successful clinical trials program is important in order to evaluate new treatments and provide access to the community. In turn, novel treatments can be brought to the market in an efficient manner. This manual describes the different aspects of clinical trial investigator sites to assist in conducting clinical trials in compliance with all applicable laws, regulations, standards and guidance. It includes a selection of essential templates to assist in operational efficiency.
Key Features
- Discussion of legal and regulatory intent
- Best practice approach to clinical research compliance
- Source and essential document templates
- Manual for entry-level as well as experienced clinical research professionals
- Potential to serve as textbook for clinical trial formal training programs
Pay easily by card, Klarna, Apple Pay or Google Pay. Not happy? You always have a 14-day money-back guarantee. Read more in our terms. If you have any questions, email us at hello@memmo.org.
Memmo makes studying easier – wherever you are in the world. We bring your course books and smart study tools together in one place: summaries, quizzes, podcasts and flashcards. Plus Ted, your study buddy who answers anything you wonder. Over 50,000 students already study here – built to help you learn faster and stress less.