Find out what The Global Health Network can do for you. Register now.
To celebrate World Health Day The Global Health Network is hosting a week of e-seminars, e-workshops and interviews that will discuss the operational, methodological and capacity challenges that impede health research in LMICs, and how to overcome common barriers.
Lecturio is a leading international eLearning platform for medical video education, serving students as well as universities and medical institutions. To offer best-in-class online medical courses, they work with hand-picked, renowned medical instructors from universities all over the world, and are offering their courses for free to all Global Health Network users.
All research studies on human subjects should have a level of quality and ethical standard assurance built into their operations to ensure that that the rights and well-being of human subjects are protected and that the data are reliable. This combined template and guide assists research teams in developing a QA plan for their study.
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 you are considering which grant to apply to. In this article we provide practical tips and information for writing grant applications, which can be applied to grant applications of all sorts, from fellowships to large funding applications.
Links to resources provided by iRIM (the Initiative on Research and Innovation Management) - free online presentations and tutorials relating to how to manage grants and perform administration of clinical research projects effectively.
New to monitoring clinical research trials? Ogundokun Olusegun outlines some of the responsibilities and tasks that the role involves, from revieiwing sites and managing research centers to the lifestyle pressures on the road.
A range of downloadable templates and tools for Clinical Research, including monitoring checklists, budget spreadsheets, informed consent forms, SOPs and so on.
What is the definition of clinical trial monitoring? Who can be a monitor? What are the monitor's roles and responsibilities? Read on for some answers.
We welcome contributions from members. Please submit an article for review by our editorial team.Upload now