A Guide to Efficient Trial Management

by The Trial Manager's Network

This Guide to Efficient Trial Management, published by the Trial Manager's Network (UK) and available freely online, is a must for all trial managers or coordinators. This link is for the 6th Edition (2018)

13th May 2018 • 5 comments

We use the example of the Gojjam Lymphoedema Best Practice Trial (GoLBeT), a pragmatic trial in a remote rural setting in northern Ethiopia, to extract lessons relevant to other investigators balancing the demands of practicality and community acceptability with internal and external validity in clinical trials.

3rd April 2018 • comment

The Nigerian Global Health Trial Conference 2018 took place on the 30th and 31st of January 2018 the Sickle Cell Centre, Idi-Araba, Lagos. The full report here is shared to allow others to experience and learn from the event.

28th February 2018 • 0 comments

We have to learn as much as we can about the benefits, risks, costs, and appropriate role of disclosing participant-level data, in service to the ultimate goal of honoring each trial volunteer's altruism.

22nd February 2018 • 0 comments

Access to regulatory data from the European Medicines Agency: the times they are a-changing

by Beate Wieseler, Natalie McGauran, Michaela F Kerekes, Thomas Kaiser

a milestone for data transparency in clinical research is within reach- it is hoped this is not unnecessarily delayed.

22nd February 2018 • 0 comments

Jimmy Whitworth calls for a more sustainable and palatable pathway be will to build consensus and to create a broad coalition.

22nd February 2018 • 0 comments

Mark Walport and Paul Brest argues that we need to ensure that research outputs are used to maximise knowledge and potential health benefits

22nd February 2018 • 0 comments

In this paper, Andrew Vickers argues that attitudes towards data sharing in the clinical trial community need to rethought, drastically

22nd February 2018 • 0 comments

A systematic review of barriers to data sharing in public health

by Willem G van Panhuis, Proma Paul, Claudia Emerson, John Grefenstette, Richard Wilder, Abraham J Herbst, David Heymann, Donald S Burke

This study looks at the challneges of data sharing globally. 

22nd February 2018 • 0 comments

Publishing the results of all clinical trials, whoever funds them, is required for ethical, scientific, economic, and societal reasons

22nd February 2018 • 0 comments

Prepublication data sharing

by Toronto International Data Release Workshop Authors

Rapid release of prepublication data has served the field of genomics well. Attendees at a workshop in Toronto recommend extending the practice to other biological data sets.

22nd February 2018 • 0 comments

Sharing health data: developing country perspectives

by Viroj Tangcharoensathien, Jirawan Boonperm, Pongpisut Jongudomsuk

Sharing data is not only about the technical dimension such as data management, repositories and libraries; developing countries are concerned about factors that impede data sharing, in particular, fairness

22nd February 2018 • 0 comments

Comparing potential commercial interests with seven specifications of relevant public interest reveals the lack of proportionality inherent in the current practices of EMA and NICE.

22nd February 2018 • 0 comments

John A. Spertus suggests that there needs to be some consideration about the practicalities of data sharing- in how it is shared, investment, and ensuring that data are appropriately analyzed 

22nd February 2018 • 0 comments

This article argues that scientists need to feel greater urgency to share their findings quickly, and they need additional avenues to facilitate this process.

22nd February 2018 • 0 comments

This paper summarises major developments in clinical trial transparency between January and June 2013 and analyses the composition of datasets released by GlaxoSmithKline.

22nd February 2018 • 0 comments

This article looks at the benefits of data sharing, and argues for increasing the accessibility of data

22nd February 2018 • 0 comments

This article details the procedures and requirements for researchers in sharing data from clinical trials. 

22nd February 2018 • 0 comments