![]() “So, we don't receive a stipend, or anything like that yet.” We’re using recording space and editing programs that are free for now,” she said. ![]() “We haven’t had to pay anything out of pocket. The university is not currently funding this podcast, Ward said, though the communications department supports the program by forwarding emails to students. The podcast is recorded at Sadleir House, a non-profit community centre on George Street North serving Trent students. “And that could also be used for incoming students to learn about different research going on in the grad studies department.” “When I came to Trent for grad school, I wanted to create something that allowed grad students to share the work they were doing,” Ward said. 10 and drops new episodes every Monday at noon.Ĭo-host Meghan Ward, in the second year of her master’s degree, formed the show with Sasha Newar, who is currently finishing the fourth year of her Ph.D. The Fellowship of the Research Podcast debuted Feb. students in the environmental and life science program at Trent University have launched a new podcast which showcases graduate student research from across all disciplines. In addition, the study physician may withdraw a participant at any time, without consent, if it becomes evident that it’s not in their best interest to continue.Two Ph.D. Throughout the trial, participants will be provided with any new information that may affect their decision to continue their involvement in the study. The wishes and best interest of the participant are considered at all times. Participants have the right to refuse participation or to withdraw their consent at any time during the study without penalty. All questions about the study should be answered to the participant’s satisfaction before an informed consent form (ICF) is signed. Participation in a clinical trial is completely voluntary. It includes an explanation of what’s involved in the trial, the duration of the study, the frequency and length of the required visits, as well as the known risks and benefits associated with the study treatment. Informed consent is the process by which a potential study participant agrees to participate in a trial after being provided with information about the study and treatment. ![]() They provide the means to develop new treatments that are as effective, more effective, or safer than treatments already on the market they enable researchers to discover new therapeutic uses for currently available medications, and they make it possible to develop innovative treatments for conditions that currently have no treatment. These studies have several development stages including early/phase I, phase IIB-III, and phase IIIB-IV research, with most phases requiring volunteers to help ensure efficacy and safety.Ĭlinical trials are important to ensure individuals receive safe and effective treatments for their health conditions, from heart disease to headaches, covering therapeutic areas like Central Nervous System, Cardiovascular, General Medicine, Rare Disease, and Oncology. The company must then select a number of medical research centers or clinics around the country that can recruit appropriate participants for the study. When a drug company wants to license a new drug, the United States Food and Drug Administration (FDA), the European Medicines Agency, and other regulatory authorities require that the drug be tested on a large number of patients to make sure the drug is both safe and effective. What are clinical trials and why are they important?
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