Course Description This course will provide an introduction to the scientific, statistical, and ethical aspects of clinical trials research. Fundamentals of Clinical Trials Free Medicine Online Course On EdX By Harvard (James Ware, Elliott Antman, Julie Buring, Graham McMahon, Marcia Testa, Robert Truog) Clinical trials play a pivotal role in evidence-based medicine. This course will discuss the design, conduct, analysis, and interpretation of Phase I-IV clinical studies. You will also stay up to date with any legislative changes in GCP as our training courses are constantly monitored, reviewed and updated. Students are introduced to the clinical research spectrum and become familiar with the essential components necessary to conduct clinical trial research in a global market. This program is designed to provide a practical context to help clinical research professionals learn about conducting clinical trials. This course will provide an introduction to the scientific, statistical, and ethical aspects of clinical trials research. (40 minutes) The clinical trial is “the most definitive tool for evaluation of the applicability of clinical research.” It represents “a key research activity with the potential to improve the quality of health care and control costs through careful comparison of alternative treatments” [1]. Fundamentals of clinical trial design. We can also offer generous group discounts on larger purchases. Fundamentals of Clinical Trials | edX Learners save time too by choosing when and where they complete the training. Advanced lecture 2: What is a clinical trial and why bother? Clinical trials play a pivotal role in evidence-based medicine. This training module provides a brief introduction on various aspects of clinical trials. UW Institute for Clinical and Translational Research, Fundamentals of Clinical Trials – Online Training, Clinical and Health Informatics Institute (CHI2), Dissemination & Implementation (D&I) Launchpad, Graduate Program in Clinical Investigation, Basics part 1: Types of studies, study questions, outcome measurements and study population choices, Basics part 2: Study design, conduct and data collection, Basics part 3: Study monitoring and analysis, Advanced lecture 1: Background and history of clinical trials. Thus careful planning with clear foresight is crucial. Please enter the number of licences required. Feedback, questions or accessibility issues: info@ictr.wisc.edu. Demonstrate leadership in clinical trial processes through evaluating clinical trial contexts and scenarios, including making recommendations that comply with good clinical practice. Fundamentals of Clinical Trials Online | Good Clinical Practice Training Course Introduction to Clinical Trials - Online Training Course This course is intended as an introduction to clinical trials for site staff who are new to clinical research and those from a non-clinical background. In the first part of the course, students will be introduced to terminology used in clinical trials and the several common designs used for clinical trials, such as parallel and cross-over designs. Abstract . Advanced lecture 6: Trial monitoring for safety and benefit (61 minutes) You can easily pay up to ten-times more for face-to-face training. Fundamentals of Clinical Trials A required course in the Certificate Program in Clinical Trials: Medical Device and Drug Development and Regulatory Affairs and Compliance, and an elective in Medical Product Development. The text is organized sequentially from defining the question to trial closeout. As a selected participant of this online course, you will learn about the spectrum of clinical and translational research from first-in-human studies to healthcare interventions implemented on a population level. The Fundamentals of Clinical Research certificate provides formal training and a practicum in research design and statistical analysis for professionals in health care, biotechnology, and in the pharmaceutical industry. This course was written by Claire Herholdt (with 18 years’ of clinical trials experience, most recently as Independent Clinical Project/Program Manager at CDS Clinical Development Services Ltd. Advanced lecture 1: Background and history of clinical trials (35 minutes) Fundamentals of Clinical Trials You must be enrolled in the course to see course content. Basics part 2: Study design, conduct and data collection (33 minutes) Learn the fundamentals of pragmatic clinical trials, including study design and basic analytic methods. These online training modules consist of recorded slide presentations prepared by David DeMets, PhD, Department of Biostatistics & Medical Informatics at the University of Wisconsin – Madison. PART 1 ONLINE EDUCATION COURSE DETAILS. These can be used to count towards the distance learning element of any scheme that comes under the umbrella of The Academy of Medical Royal Colleges or any other scheme for which there is mutual recognition. CPTR required 16-credit curriculum: The CPTR has a competency-based curriculum that requires 15 core and 1 or more elective credits. Build a Solid Foundation to Master Clinical Research. Since the questions are picked randomly from a database, re-sitting the exam doesn’t mean taking the same questions again and again. The course will explain the basic principles for design of randomized clinical trials and how they should be reported. Clinical Trial Fundamentals eLearning Program (all three modules!) It is also ideal for staff who need a grounding in the clinical trials process without the need for a full ICH GCP course. Learn the fundamentals of clinical research in this two-day classroom course. Topics include the design, implementation, and analysis of trials, including first-in-human studies (dose-finding, safety, proof of concept, and Phase I), Phase II, Phase III, and Phase IV studies. A comprehensive guide to the practical application of International ICH-GCP. The Introduction to the Principles and Practice of Clinical Research (IPPCR) course trains registrants on how to effectively and safely conduct clinical research. It is important that everyone involved in research is trained or appropriately experienced to perform the specific tasks they are being asked to undertake. Topics include the design, implementation, and analysis of trials, including first-in-human studies (dose-finding, safety, proof of concept, and Phase I), Phase II, Phase III, and Phase IV studies. The Part 1 "Education" consists of a comprehensive online course covering chapters one through seven. Sign in or register and then enroll in this course. This series of lectures covers similar topics as the basics course above, but explores each topic in greater detail. Key decisions surrounding design (including sample size), delivery and assessment of clinical trials will be explored. Advanced lecture 5: Sample size estimation (52 minutes) This course is an introduction to the international ICH-GCP guidelines, providing practical interpretation for those new to clinical trials. Covers similar topics as the basics course above, but explores each topic in greater detail program ( all modules. Constantly monitored, reviewed and updated of pragmatic clinical trials are a result of poor.... Viewed at your own pace our reporting tools make it easy for administrators to check the progress of and. Without the need for a full ICH GCP course need a grounding in the clinical trial and bother. 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