A new, open-access toolkit for researchers and data managers is released today, providing guidance, resources and an eLearning course about ethics and best practices of sharing individual-level health research data in LMICs. This resource is a key output from a ... Read more
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Global Health Trials has released an improved, updated, quality reviewed set of over 120 templates and SOPs for clinical research - everything from informed consent templates to contracts, checklists, logs and lab SOPs. These have all been donated from research ... Read more
The Institut Pasteur, a historical institution in the field of vaccine development, is launching for the first time this year a Massive Open Online Course (MOOC) in Vaccinology, which will be available on September 17, 2015. This MOOC is organized ... Read more
Field trials of interventions against disease in low and middle income countries (LMICs) may be complex and expensive undertakings. The 3rd edition of “Field Trials of Health Interventions: a Toolbox” has been compiled by over 30 contributors with extensive direct ... Read more
Ethics of Ancillary Care in Research is a free, online, open access training course developed by The Global Health Network and our latest member site Bioethics, Research Ethics & Review. This short course provides an overview of ancillary care in ... Read more
The Research to Publication programme is part of BMJ's commitment to building medical research capabilities around the world. The programme is designed to be modular and new courses will be added over the coming months. The first module, How to ... Read more
Clinical research involving children is essential to increase our understanding of childhood conditions and improve healthcare for children. Yet professionals and parents often feel uneasy about asking children to take part in research, for example because of potential risks or ... Read more
Sharing individual-level data in low and middle income settings - special issue and online eLearning course
A Special issue of the Journal of Empirical Research on Human Research Ethics, launched today, focuses on the ethical implications of sharing health research data in low and middle income settings. To accompany the special issue, Bioethics, Research Ethics & Review has launched an online resourcewhich brings together resources about ethical best practices for data sharing, policies and processes for data curation and data sharing, and links to repositories for data sharing.
We'd like to invite you all to take part in the next WorldWide Seminar during August on the subject of Statistics.
The WorldWide Seminar Series is a very simple ...
Global Health Trials is launching a new campaign - Share1Thing - to encourage researchers to share just one tip, SOP, template, resource, or any other item from their trials, so as to ...
Hi everyone, this new group is a place for new members to introduce themselves in the community. Please post to introduce yourself and let others know about where you are ...
Introduction: All quantitative clinical research studies and clinical trials, from observational epidemiology studies to large phase III or IV global trials of new drugs, produce data. These data are produced ...
Click here for Spanish version Grant applications differ substantially depending on the individual funding organisation, and each funding organisation has its own organisational aims, which are important to understand when ...
Global Health Trials Careers Month Job interviews can be intimidating, but simply preparing well can make the difference between succeeding or failing, regardless of how nervous you are. In this ...
I completed my nursing education from a nursing school of India and never did I imagine that I would be a research nurse. At that time I guess the role ...
Welcome to Global Health Trials' tools and templates library. Please note that this page has been updated for 2015 following a quality check and review of the templates, and many ...
This peer reviewed course outlines ethical aspects of sharing individual level research data and proposed best practices. It aims to be of value to those designing and reviewing individual research protocols where data sharing is anticipated, and to those developing institutional policies and processes for governing data sharing.