Product News
|
- 04/01/2007 12:00:00 - Infonetica Awarded Tender to Develop UK Integrated Research Governance Form Infonetica has been awarded a tender to develop the UK Integrated Research Governance Form. Experience in developing and maintaining the National Research Ethics Service electronic form form strong backbone for bid. learn more |
|
- 30/08/2006 12:00:00 - Improvements to UK Research Ethics Recognised COREC has published a list of positive comments regarding the UK Ethics System - which is underpinned by Infonetica's software. learn more |
|
- 29/06/2006 12:00:00 - Infonetica selected as software suppliers for CIHR grant Infonetica are selected to help design and implement a system for standardised ethical review in Canada. Read the summary of the proposal... learn more |
|
- 10/08/2005 12:00:00 - Infonetica to Host International Conference on Research Ethics/IRB Activity Infonetica Ltd are hosting a two day workshop focusing on how best to support the activities of Research Ethics Committees and applicants to Research Ethics Committees in Europe learn more |
|
- 28/01/2005 12:00:00 - Delegates Identify Common Ground for European Action in Research Ethics For a research ethics committee to perform its role effectively, knowledge of the scientific and ethical issues themselves is only part of the story. The standard procedures by which a committee operates are equally crucial, and in this there also appears to be marked variation between countries. Dr Fuchs revealed that many survey respondents had asked for a database of resources for the administration of RECs, of the kind now provided by Infonetica. The ethics committee administration system (RED) - developed in the UK but now available to all countries - helps administrators to manage every aspect of the application processes, including provisional decisions, rejections, approvals, and amendments. learn more |
Infonetica Contribute to Improving the UK Clinical Research Environment
Dated: 16/06/2009 12:00:00
Infonetica software forms the basis of a number of systems improving the clinical research environment in the UK. Once again, the IRAS and CSP initiatives have been recognized - both of these systems are built around Infonetica software (ReDA for research management and the Online Form Framework for IRAS):
"But this spring, she says a number of new policies have come into force that could truly fulfil the need to make conducting trials in England a lot of simpler, faster and cheaper.
On 1 April this year a new single national method for gaining approval to conduct trials with the NHS was launched, and some success can already be seen.
The NIHR Coordinated System for gaining NHS Permission (NIHR CSP) is aimed at standardising and streamlining the process for gaining NHS Permission in England, reducing both approval times and bureaucracy.
The first two industry studies approved under the new system this year took less than 90 days from notification to the first patient visit, compared to an average time of 173 days in 2007.
Davies said: "The early signs are that the turnaround times, which are one of the issues the industry worry about, have been reduced. We believe as the training improves that it will reduce even more."
More info: http://www.pharmafocus.com/cda/focusH/1,2109,22-0-0-0-focus_feature_detail-0-492865,00.html