Overview of UW Clinical Trial Office Budget Review
UW Clinical Trial Office conducts budget reviews to ensure compliance and financial accountability in clinical trials. The office collaborates with various departments to manage billing compliance, financial risks, and institutional policies. The primary focus is on avoiding patient billing errors,
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India Alliance Clinical & Public Health fellowship in India
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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Ethical Issues in Clinical Pharmacy Research by Dr. Haider Raheem Mohammad
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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Advanced Clinical Practice Framework and Pillars of Practice
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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Objective Structured Clinical Examination (OSCE): A Modern Approach to Assessing Clinical Competence
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 Clinical Research Education and Monitoring Program Overview
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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Understanding Non-Aqueous Solvents: Types and Classification
Inorganic non-aqueous solvents play a crucial role in chemical research and industry. This article by Dr. Princy K.G. delves into the classification of solvents based on protonicity, polarity, and aqueous vs. non-aqueous nature. It explores the types of non-aqueous solvents, such as protonic and non
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Understanding Statistical Methods for Clinical Endpoints in Diabetes Research
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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Clinical Research Updates and Administrative Fee Changes
This update covers significant changes in clinical trial administrative fees, aiming to reduce burdens on the research community. The new fee structure includes a flat fee for new studies and additional charges for subject enrollment during IRB renewal. Furthermore, a new coverage analysis process h
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Understanding Non-Clinical Development in Therapeutic Innovation
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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Understanding Post-Authorisation Safety Studies (PASS) in Pharmacovigilance
Post-Authorisation Safety Studies (PASS) are conducted after a medicinal product is authorized to gather more safety information or assess risk management effectiveness. These studies evaluate the safety and benefit-risk profile of the product, aiding regulatory decision-making. PASS aims to identif
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Understanding Clinical Trials: Types and Designs
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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Understanding Non-Firm Quantities in Electricity Markets
Non-Firm Quantities in electricity markets involve units with non-firm access not being compensated for their non-firm capacity not getting accommodated on the system. The concept of Firm Access Quantity plays a key role in determining compensation levels for units, with differences in implementatio
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Understanding Non-Compete Agreements: Enforceability and Requirements
Non-compete agreements are commonly used in the United States to protect businesses from competition by former employees. To be enforceable, these agreements must meet certain requirements, including independent consideration, protection of legitimate business interests, and reasonableness in scope,
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Understanding Evidence-Based Medicine and Clinical Decision-Making
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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General Clinical Research Unit (GCRU) Services Overview
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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Essential Aspects of the Clinical Interview in Psychology
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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Deanery of Clinical Sciences Funding Challenge 2018 Launch Event
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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Critical Evaluation of Clinical Studies and Guidelines
Understanding the need to critically evaluate studies, different study types aiding clinicians, bias and random errors affecting study outcomes, finding reliable studies, and the importance of meta-analyses in clinical practice guidelines. Emphasizing the significance of evidence-based decision-maki
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Enhancing Human Subjects Research Through NIH Policy Changes
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 Guidelines and Regulations Overview
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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Insights into Cardiac Research: Metabolic Syndrome and Acute Myocardial Infarction Studies
Explore the latest findings in cardiac research focusing on two critical clinical problems: Metabolic Syndrome (MetS) and Acute Myocardial Infarction. The studies involve human clinical data, blood sampling, adipose tissue biopsies, cell culture studies, thrombus aspiration, gene arrays, and regulat
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Essential Elements of Clinical Trial Protocols
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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Hematological Cancer Clinical Studies Update and Recruitment Statistics
Latest update on hematological cancer clinical studies from the SWAG.Network Haematological Cancer Clinical Advisory Group, including national recruitment data, regional recruitment comparisons, open studies, and sample size information for ongoing studies. This comprehensive update covers a range o
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Ohio Clinical Alliance: Transforming Clinical Experiences
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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Advances in Baryon Spectroscopy and Hadronic Matter Studies
Discussions at the meeting focused on interpreting HADES results for e+e- and meson production in hadronic reactions, with studies involving proton, pion, light, and heavy ion beams. The role of time-like electromagnetic transitions, baryon spectroscopy, and connecting hadronic matter studies were e
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Sponsor Expectations for Clinical Studies at Thomas Jefferson University
This presentation discusses the sponsor expectations for clinical studies, investigator responsibilities, TJU's strengths in conducting studies, and how principal investigators can impress sponsors. Topics include assessment of investigator performance, regulatory guidelines, streamlining processes,
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Safety Practices and Reporting in Clinical Research
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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Exploration of Endpoints in Clinical Trials for Alcohol Use Disorder
This presentation discusses the exploration of endpoints in pivotal clinical trials to treat Alcohol Use Disorder (AUD), focusing on Primary Alcohol Drinking Endpoints like PSNHDD. Evidence supporting PSNHDD as a primary endpoint includes clinical benefit data from alcohol clinical trials and epidem
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Perception and Awareness of Clinical Research in Trial Participants and the Public of Andhra Pradesh
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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Understanding Targeted Clinical Investigation in Pharmacovigilance
Targeted clinical investigation plays a crucial role in pharmacovigilance by further evaluating significant risks identified in pre-approval clinical trials. This involves conducting pharmacokinetic and pharmacodynamic studies, genetic testing, interaction studies, and large simplified trials to ass
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Pain Opioid Actively Managed Portfolio (POp.AMP): Research Advisory Committee Overview
The Pain Opioid Actively Managed Portfolio (POp.AMP) focuses on addressing pain, opioid addiction, and suicide prevention through proactive management, agile funding mechanisms, and collaboration with various stakeholders. The committee utilizes a rotational leadership model to ensure efficient rese
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Breast Cancer Clinical Research Update: Key Findings and Studies Overview
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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Comparison of Professional Behaviors in Clinical Education
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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Adventist Health Studies Contributions & Collaborations Overview
Adventist Health Studies have made significant contributions to understanding the health and longevity advantages of Seventh-day Adventists, particularly focusing on vegetarian diets and cardiovascular health. With a history spanning over 57 years and various cohort studies, these studies have provi
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Enhancing Clinical Academic Collaboration Between Universities and NHS Trusts
Clinical academics play a crucial role in integrating clinical practice, research, and education within the NHS. Collaboration between universities and NHS trusts is key to ensure clinical academics address the right questions for patient care and societal benefit. Challenges include an aging clinic
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NHMRC's New Grant Program: Advancing Clinical Trials and Research Funding
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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SWAG Network Oesophago-gastric Cancer Research Update
SWAG Network Oesophago-gastric (OG) Cancer Clinical Advisory Group provided a research update on Upper GI Cancer Studies, National Recruitment data, and Regional Recruitment trends in the UK. The update included information on open cancer studies, sample sizes, recruitment statistics, and participat
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Understanding Clinical Trials: Phases, Types, and Definitions
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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Clinical Research Workflow Optimization Overview
Clinical research workflow optimization aims to streamline the process of subject enrollment, study approval, and Epic integration. It involves linking encounters to research studies, using automated tools for transactional data, and enhancing the research workqueue training. The process includes au
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