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Clinical data management (CDM) is a critical process in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials. [1] Clinical data management ensures collection, integration and availability of data at appropriate quality and cost.
A protocol describes what types of people may participate in the trial; the schedule of tests, procedures, medications, and dosages; and the length of the study. While in a clinical trial, participants following a protocol are seen regularly by research staff to monitor their health and to determine the safety and effectiveness of their treatment.
A standard operating procedure (SOP) is a set of step-by-step instructions compiled by an organization to help workers carry out routine operations. [1] SOPs aim to achieve efficiency, quality output, and uniformity of performance, while reducing miscommunication and failure to comply with industry regulations .
A clinical research associate (CRA), also called a clinical monitor or trial monitor, is a health-care professional who performs many activities related to medical research, particularly clinical trials. Clinical research associates work in various settings, such as pharmaceutical companies, medical research institutes and government agencies.
The Walter Reed Tropical Medicine Course (now called 'Operational Clinical Infectious Disease' Course) at Walter Reed Army Institute of Research (WRAIR) is one of the many Tropical Medicine Training Courses available in the US and worldwide (see Tropical medicine). It is an intensive 5-day course and a 3-day short course, created to familiarize ...
OpenCourseWare (OCW) are course lessons created at universities and published for free via the Internet.OCW projects first appeared in the late 1990s, and after gaining traction in Europe and then the United States have become a worldwide means of delivering educational content.
In late 2023, Vivance pulled in a second round of funding worth $20 million in preparation for a U.S.-based clinical trial. Qidni Labs in Buffalo, New York, is also developing a sorbent-based ...
Similar to clinical research, preregistration can help to improve transparency and quality of research data in preclinical research. [46] [47] In contrast to clinical research where preregistration is mandatory for vast parts it is still new in preclinical research. A large part of preclinical and basic biomedical research relies on animal ...
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