Recent Discussions
FDA requests comments: Clinical Trials Registration and Results Submission
The FDA is seeking comments on its requirements for submitting registration and summary results information, including adverse event information, for specified clinical trials of drugs (including biological products) and devices and for ...
One Day Skills-Sharing workshop in Dar es Salaam on Clinical Trials in Tanzania - all welcome, free to attend (but please register!)
Just a reminder that if you would like to register for the one-day skills sharing workshop in Dar on 12th July, please email me at info@globalhealthtrials.org to do so; places are filling ...
Recent Blog Posts
Clinical Data Management
Why does the industry require Clinical Data Management?The industry requires Clinical Data Management because drugs, treatment methods, vaccines etc. ate ...
Enteric Viruses Protocol build up thoughts
I have this idea of getting a protocol developed by like minded guys on the enteric viruses. I have made ...
12 top tips for writing a grant application from the MRC
Sitting down to write a grant application? Recently submitted a proposal or been successful in the last MRC board round? ...
Lassa Fever outbreak! Any research response?
Since 1968, Lassa fever has been a scourge. The fire keeps burning unabated. There is currently another outbreak. But the ...
New e-Learning Module! GCLP: Module 5 - Method & Systems Validation
Good Clinical Laboratory Practice (GCLP) is a free, online, multi-module training course developed by The Global Health Network and the ...