Clinical trials regulatory training

Listing Results Clinical trials regulatory training

3 hours ago Clinical Investigator Training Course. Free online courses for state, local, and tribal regulatory partners. FDA 101: An Overview of FDA's Regulatory Review and …

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3 hours ago Online training on human subject protection provided by HHS’ Office for Human Research Protections. Clinical research training is a course developed by the National Institutes of Health to train

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7 hours ago Regulatory Training for Clinical Research Professionals. OVERVIEW: There is a lack of qualified clinical research professionals skilled in clinical trial regulatory management in the academic setting. In addition, professional

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4 hours ago Official website of the National Institutes of Health (NIH). NIH is one of the world's foremost medical research centers. An agency of the U.S. Department of Health and Human Services, the NIH is the Federal focal point for health and medical research. The NIH website offers health information for the public, scientists, researchers, medical professionals, patients, educators, …

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6 hours ago In summary, here are 10 of our most popular clinical trials courses. Design and Interpretation of Clinical Trials: Johns Hopkins University. Data Management for Clinical Research: Vanderbilt University. Clinical Data Science: University of Colorado System. Understanding Clinical Research: Behind the Statistics: University of Cape Town.

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1 hours ago SOCRA has implemented an online component to the already robust array of educational opportunities. These online courses offer affordable, convenient access to quality education. SOCRA's online courses are intended to provide access to training and continuing education that will promote quality clinical research, protect the welfare of research

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7 hours ago Introduction to Clinical Trials is an ideal program for all novice clinical researchers, those interested in the profession, or those indirectly involved in clinical trials. This course provides the foundational knowledge upon which one can develop his/her competence as a clinical research professional. This two-hour online course details how

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9 hours ago The Association of Clinical Research Professionals (ACRP) supports clinical research professionals through membership, training and development, and certification. Founded in 1976, ACRP is a Washington, DC-based non-profit organization with more than 13,000 members who work in clinical research in more than 70 countries.

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5 hours ago About this course. This course is based on the international E6 ICH Good Clinical Practice regulations and is a complete training solution for all individuals that need to acquire GCP knowledge. Our free GCP training can also serve …

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7 hours ago SOCRA offers a robust portfolio of live in-person conferences, workshops, and courses to keep you at the forefront of the industry and support your continuing educational goals. See below for a full list of live programs, or visit the event calendar. CCRP Preparation and GCP Review Course.

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Just Now Free Regulatory Affairs E-learning Course Module. Posted on 05/01/2019 22/03/2021 by ilearngira. Free Regulatory Affairs E learning Course Module. Courses. Computer System Validation Training (CSV) Advance Drug Regulatory Affairs Program; ECTD TRAINING; Free Regulatory Affairs E-learning Course Module; Medical Device Regulatory

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2 hours ago The principles of Good Clinical Practice (GCP) help assure the safety, integrity, and quality of clinical trials by addressing elements related to the design, conduct, and reporting of clinical trials. GCP training describes the responsibilities of investigators, sponsors, monitors, and IRBs in the conduct of clinical trials. GCP training aims

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6 hours ago 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. We will also explain some of the mechanics of clinical trials, like randomization and blinding of treatment. In the second half of the course, we

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6 hours ago 13 July 2022. The Institute of Clinical Research Training Suite. THIS COURSE HAS BEEN POSTPONED. This course provides an in-depth look at the regulatory systems currently in operation in the EU and their impact, together with UK legislation, on the conduct of clinical research. Starting with a refresher on the history of medicinal product regulations and the …

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6 hours ago Navigate the European (bio)pharmaceutical regulatory landscape to meet and maintain compliance under the Clinical Trials Regulation with the help of this focused 2-day online training course, 19-20 September 2022. The Clinical Trials Regulations: Navigate The European (Bio)Pharmaceutical Regulatory Landscape To Meet And Maintain Compliance …

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4 hours ago About This Program. Clinical Trials are a key tool in the evaluation of new strategies for prevention and treatment of disease. This certificate program focuses primarily on the design and analysis of randomized clinical trials for evaluation of licensed and non-licensed medical products and other health interventions, the regulatory framework

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Just Now There are no background requirements in terms of education, knowledge, or experience, just an interest in clinical research with human subjects. This course is readily accessible to the non-medically trained as well as to those in the field of scientific research. As a rule, background education includes a mix of MD, PhD, RN, MPH, MSW, MPH, and BA/BS. Cost. There is no …

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Frequently Asked Questions

Where can I find clinical trials management and monitoring training courses?

Biopharma Institute offers a catalog of over 200 programs for pharmaceutical, medical device, and clinical research professionals. Below is our list of Clinical Trials Management and Monitoring training courses and professional certification programs. Free Course: Start Learning, Today! Learn more

Is this course suitable for everyone involved in clinical research?

This course is suitable for everyone involved in clinical research. - This course outlines the role of a Data Safety and Monitoring Board (DSMB) during a clinical trial. Appointed by the trial's sponsors, the DSMBs are responsible for assessing the overall progress of the trial and focusing in particular on analysing the safety and efficacy data.

What is an introduction to clinical trials and clinical trial practice?

An Introduction to Clinical Trials and Clinical Trial Practice, the ICR’s flagship training course, is accredited by Cranfield University. This highly practical course explores the relevance of clinical research in drug development and summarises the ethical and regulatory requirements for clinical trials.

What is the curriculum of the clinical trials management online certificate?

The curriculum of the Clinical Trials Management Online Certificate covers core concepts consistent with the Association of Clinical Research Professionals (ACRP) certification exams, a valuable credentialing opportunity for clinical research professionals.


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