clinical trial application

  • 1Clinical trial — Clinical trials are a set of procedures in medical research and drug development that are conducted to allow safety (or more specifically, information about adverse drug reactions and adverse effects of other treatments) and efficacy data to be… …

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  • 2Clinical trial management — A clinical trial is the application of the scientific method to human health. Since such trials require the use of human test subjects and can severely impact the well being of the subjects, as well as treatments of other people and large amounts …

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  • 3Clinical Trial Portal — Not to be confused with Clinical Trials Registry or Clinical Trial Management System. A clinical trial portal (also known as clinical portal or clinical study portal) is a web portal or enterprise portal that primarily serves sponsors and… …

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  • 4Clinical research — is a branch of medical science that determines the safety and effectiveness of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving… …

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  • 5Clinical data management — encompasses the entry, verification, validation and quality control of data gathered during the conduct of a clinical trial. Contents 1 Role of the Clinical Data Manager in a Clinical Trial 2 Standard Operating Procedures 3 The Data Management… …

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  • 6Clinical decision support system — (CDSS or CDS) is an interactive decision support system (DSS) Computer Software, which is designed to assist physicians and other health professionals with decision making tasks, as determining diagnosis of patient data. A working definition has… …

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  • 7Clinical research coordinator — The Clinical Research Coordinator (CRC) is responsible for conducting clinical trials using good clinical practice [1] (GCP) under the auspices of the Principal Investigator (PI). Good Clinical Practices Principles have been defined by Madelene… …

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  • 8Clinical trials with surprising outcomes — Medicine is an evolving field as new knowledge is acquired through discoveries in the laboratory and through clinical trials. With the acceptance of evidence based medicine, some practices that were thought to be standard of care or represent… …

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  • 9Clinical Trials Directive — The Clinical Trials Directive (Officially Directive 2001/20/EC of 4 April 2001, of the European Parliament and of the Council on the approximation of the laws, regulations and administrative provisions of the Member States relating to… …

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  • 10Clinical pharmacology — is the science of drugs and their clinical use. It is underpinned by the basic science of pharmacology, with added focus on the application of pharmacological principles and methods in the real world. It has a broad scope, from the discovery of… …

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