India Alliance Clinical & Public Health fellowship in India\n\nIndia Alliance Clinical and Public Health Research Fellowships are for Health researchers with an MD, MS, MPH, or an equivalent clinical or public health degree, who can apply for the DBT\/Wellcome Trust India Alliance Clinical and Publi

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Clinical psychology training models such as the Scientist-Practitioner Model have evolved over the years to integrate science and practical expertise. The Scientist-Practitioner Model, originating in 1949, emphasizes the fusion of scientific knowledge and clinical application. It faced criticism for

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Research ethics play a crucial role in clinical trials and therapeutic research in the field of pharmacy. From discovery to validation, all medicines undergo rigorous evaluation processes to ensure safety, efficacy, and freedom from adverse effects. Clinical trials in both animals and humans are ess

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The document discusses the advanced clinical practice framework and the four pillars of practice which include leadership & management, clinical practice, education, and research. It emphasizes the importance of core capabilities and area-specific competence in advanced clinical practice. The role o

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This session discusses the landscape of DHT-derived novel endpoints in clinical research, focusing on considerations for regulatory decision-making. It explains the use of digital health technology in clinical outcome assessments and highlights the potential benefits of digitally collected COAs, suc

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The Objective Structured Clinical Examination (OSCE) is a modern examination method widely used in the field of health science to evaluate clinical skill performance. It involves stations where medical students interact with simulated patients to demonstrate competencies such as history taking, phys

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NIMH's Clinical Monitoring and Clinical Research Education, Support, and Training Program (CREST) aims to ensure the proper conduct, recording, and reporting of clinical trials. This program includes clinical monitoring plans, guidelines for site monitoring activities, and independent clinical monit

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This educational slide module delves into fundamental statistics for analyzing clinical endpoints in diabetes research. It covers the choice of statistical methods, the distinction between statistical and clinical significance, and the importance of different endpoints in evaluating clinical benefit

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Explore the historical context, important ethical guidelines, and the ethical framework with 7 principles in the field of clinical trials. Learn about key trials, ethical considerations, and guidelines governing human subject research in clinical medicine. Delve into the critical aspects such as inf

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The European Patients Academy on Therapeutic Innovation focuses on the non-clinical development phase of medicine, delving into efficacy assessment, safety evaluation, and manufacturing process considerations. Non-clinical studies are essential for decision-making in clinical trials, marketing appli

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SOCRA is a non-profit organization dedicated to providing education, certification, and networking opportunities in clinical research. Established in 1991, it offers workshops, conferences, and a CCRP program for industry professionals. Attendees benefit from experienced presenters and opportunities

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Explore Epic tools for clinical research developed by Shara Power, a skilled application developer specializing in EPIC Beacon Oncology at UIHC Healthcare Information Systems. Learn about managing research study records, investigational study medication orders, and the process for creating and using

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Epic Tools for Clinical Research, developed by Shara Power, RN, BSN, OCN, offers a comprehensive suite of applications within the EPIC system for managing research study records, medication orders, treatment plans, billing, consent records, and patient associations. This solution streamlines the pro

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The BMC Clinical Trials Office (CTO) is dedicated to supporting clinical and human research at Boston Medical Center by providing leadership and expertise in research, finance, and administration. The CTO reviews, negotiates, and approves protocols, supports grants and contracts, ensures accurate cl

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Clinical trials are essential research studies that evaluate new tests and treatments to improve human health outcomes. They involve various phases, designs, and purposes, such as treatment trials, prevention trials, and observational studies. Different types of clinical trial designs include experi

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Translational research aims to translate basic scientific discoveries into practical applications for patient care. This involves moving research from the laboratory to clinical settings effectively and safely. Key aspects include designing studies using relevant models, documenting mechanisms of ac

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European Patients Academy on Therapeutic Innovation emphasizes the importance of Evidence-Based Medicine (EBM) in providing optimum clinical care. EBM involves systematic review and utilization of clinical research for informed decision-making, benefiting patients in disease management and treatment

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Clinical research professionals can utilize EPIC tools and processes to streamline study management, patient association, and research data tracking. The system enables the creation of study-specific research records, patient associations, and detailed study descriptions. From building research stud

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The General Clinical Research Unit (GCRU) under Ridiane Denis offers support for a wide range of active protocols in various research areas like endocrinology, Alzheimer's, oncology, and more. GCRU provides clinical and laboratory services including sample processing, infusion, biopsy, urine analysi

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Clinical interviews play a crucial role in the assessment conducted by clinical psychologists, showcasing essential qualities like validity, reliability, and clinical utility. Understanding the importance of feedback and honing general and specific skills as an interviewer are key components in cond

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The Deanery of Clinical Sciences is offering a small grant opportunity for early career researchers within the clinical sciences field. The fund aims to support researchers' current studies and research projects with a maximum grant of £2,500. Applications are open to postgraduates and postdocs, an

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The National Institutes of Health (NIH) is implementing reforms and initiatives to improve the stewardship of research involving human subjects, particularly in the context of clinical trials. These changes include new forms for data collection, training in Good Clinical Practice, use of a single In

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Clinical research encompasses various guidelines and regulations to ensure the protection of human subjects and the credibility of study results. Key aspects include Good Clinical Practice (GCP) standards, Title 45 of the Code of Federal Regulations (CFR) Part 46, and additional CFR sections for cli

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Understanding the key components of a clinical trial research protocol is essential for conducting successful studies. This includes identifying session objectives, discussing trial protocol contents, exploring observational study elements, and learning about reporting guidelines. Study objectives f

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This document presents a Clinical Judgement Test focusing on the relevance of a research question and the appropriateness of the study design. Candidates are evaluated on their critical review skills and ability to assess both strengths and weaknesses of the research methodology employed. The test a

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The Ohio Clinical Alliance, through collaborative partnerships, aims to enhance clinical preparation for educators. The leadership team comprises various representatives and organizations committed to improving student learning. Their activities include retreats and meetings to ensure effective comm

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Learn about Good Data Management Practice (GCDMP), Good Documentation Practice, and Good Storage & Archiving Practice in clinical research. Understand the significance of data, key data collection processes, best practices for reporting data in CRF, importance of documentation, and data storage/arch

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This presentation showcases survey data on various aspects of research training and educational support in clinical research environments, including questions on being a Principal Investigator, managing research staff, training adequacy, study types, tenure at the University of Chicago, training pre

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Safety practices and reporting in clinical research are crucial for ensuring the rights, safety, and well-being of trial subjects. This includes monitoring safety, reporting adverse events promptly, and following regulatory requirements. Investigators play a vital role in assuring subject safety and

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Explore the Clinical Trials Transformation Initiative's efforts in updating ICH E6 guidelines to improve global clinical trials. Learn about CTTI's findings, insights from stakeholders, and discussions on the necessary updates for ICH E6. Engage with industry experts and regulatory authorities to un

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Explore the recent Clinical Research Support Services Town Hall event featuring presentations on various core services, breakout rooms for inquiries, and details on biospecimen repository and biobanking services provided by Wayne State University. Learn about the mission, high-quality biospecimens a

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Explore the fascinating journey into clinical research as Dr. Emma Pagnamenta, a Research Manager at RCSLT, delves into linking genes with brain development and behavior. From special schools in Birmingham to mainstream and early years in Wandsworth and Oxfordshire, discover the importance of a clin

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This study focuses on understanding the perception and awareness of clinical research among trial participants and the general public in Andhra Pradesh. It highlights the importance of creating awareness about clinical research, previous study results, public attitudes towards clinical trials, and e

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Clinical psychology, first introduced in 1907, encompasses a diverse field focusing on the study, assessment, and treatment of psychological issues. The APA Division 12 defines clinical psychology as integrating science, theory, and practice to understand and alleviate maladjustment. Training typica

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Clinical Education Research delves into various aspects such as teaching, learning strategies, learner wellbeing, professional regulation, and career paths within the clinical education domain. This research explores methods like surveys, interviews, realist reviews, and workplace interventions to e

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The SWAG.Network Breast Cancer Clinical Advisory Group Research Update by Claire Matthews discusses the latest developments in breast cancer studies from April 2020 to March 2022. It covers national recruitment data, comparison between national and regional recruitment, and details of ongoing studie

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This content provides an overview of clinical trials, including the goals, phases, study funding, and important terms such as placebo. Clinical trials aim to study the impacts of health and disease, evaluate treatments, and ensure safety and effectiveness. The phases of clinical trials are explained

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Professional behavior characteristics play a crucial role in enhancing student learning during clinical education. This study examines the differences in reported importance and frequency of professional behaviors between credentialed and non-credentialed clinical instructors. The background outline

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The NHMRC's latest grant program aims to enhance research in healthcare by focusing on clinical trials funding across four key streams: Investigator Grants, Synergy Grants, Ideas Grants, and Strategic and Leveraging Grants. The redistribution of funding will see a significant increase in support for

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Clinical trials play a crucial role in advancing medical research and treatment options. This comprehensive guide covers the basics of clinical trials, including their definition, phases, types, and key definitions like IND, IDE, NDA, and more. Discover how different phases of trials work, the vario

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