Titlebook: Biomedical Product Development: Bench to Bedside; Babak Arjmand,Moloud Payab,Parisa Goodarzi Textbook 2020 Springer Nature Switzerland AG

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https://doi.org/10.1007/978-0-387-78864-7justification of the research – especially ethical wise – and establishment of procedures for documentation. Further, the risk management processes and principles are other essential parts of GCP which will be addressed. Finally, the most important challenges and different ways to overcome them will be introduced.

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Good Clinical Practice: Guidelines and Requirements,justification of the research – especially ethical wise – and establishment of procedures for documentation. Further, the risk management processes and principles are other essential parts of GCP which will be addressed. Finally, the most important challenges and different ways to overcome them will be introduced.

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https://doi.org/10.1007/978-0-387-78864-7e participants will be demonstrated, and intervention includes concepts like diagnostic intervention. Furthermore, a snapshot of clinical trial monitoring, risk assessment, and its various types will be exhibited with a brief focus on registration and obstacles.

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Principles of Good Clinical Practice,hich you will be faced with using the guidelines, there are some examples about different kinds of GCP guidelines around the world to show how it is implemented and influences the performance and management of clinical trials.