Research Application System News Today

Years. British Prime Minister David Cameron is to live in china on monday beating one hundred strong trade delegation to bolster business. December marks World Aids Day twenty years kelly during baht in new hiv infections and rear brake and gas will want. The law come from a genial watching cctv new zine bomb among thai Anti Government protesters have rejected the armys offered to mediate talks to restock the current political conflicts. Well classes in bangkok have left at least two people dead...

The new MHRA scheme helps to reduce the time it takes for the lowest-risk clinical trials to commence, while maintaining patient safety.

Objective To determine the effectiveness of an exercise and functional activity therapy intervention in adults with early dementia or mild cognitive impairment compared with usual care. Design Randomised controlled trial. Setting Participants’ homes and communities at five sites in the United Kingdom. Participants 365 adults with early dementia or mild cognitive impairment who were living at home, and family members or carers. Intervention The intervention, Promoting activity, Independence, an...

In low- and middle-income countries, poverty and impaired growth prevent children from meeting their cognitive developmental potential. There are few studies investigating these relationships in high-income settings. Participants were 12,536 children born between 2000 and 2002 in the UK and participating in the Millennium Cohort Study (MCS). Short stature was defined as having a height-for-age 2 or more standard deviations below the median (≤ − 2 SDS) at age 3 ye...

The Medicines & Healthcare products Regulatory Agency (MHRA) launched a consultation in early 2022 as part of its post-Brexit efforts to develop a…

Last week the Regulation on Clinical Trials (“CTR”) finally became effective in the European Union (“EU”) and replaced the prior Clinical Trials Directive 2001/20 (“CTD”). The CTR was...

The UK Medicines and Healthcare products Regulatory Agency (MHRA) has launched a public consultation to improve and strengthen UK clinical trials legislation.

Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.

How and when to submit research applications to ARSAC Guide to submitting research applications to the Administration of Radioactive Substances Advisory Committee (ARSAC). From: Contents ARSAC) research approval for all your research projects where the protocol: requires the administration of radioactive substances specifies the frequency, activity or processing for an administration that would otherwise be considered standard care You do not need to obtain ARSAC research approval fo...