Infonetica Research Solutions



Infonetica provides a global leading range of Clinical Research Solutions including Clinical Research  Application and Management Systems, Institutional Review Board (IRB) Software, Research Management Software, and Human Tissue Tracking Software. Infonetica products are in use in the UK at both national and local levels, and internationally, with government and private sector contracts in Europe, US, Canada and Australia.

 A unique product set has been developed that assists in streamlining processes, and crucially reducing clinical trial start up times. A major factor contributing to slow clinical trial start up times is the time taken for pharmaceutical companies and other applicants to obtain permissions. These have to be given by ethics committees, participating sites, specialist regulatory authorities and other relevant bodies.

Infonetica’s core product set has helped establish a cohesive approach to processing application data and obtaining permissions. Their high profile products have been adopted at national and regional levels globally, and have resulted in huge efficiencies together with vastly improved permission times.                                                                                         

Infonetica products are fully supported by helpdesk services, sector knowledge, consultancy and dedicated training specialists.

Infonetica Products - Research Software

RED - Research Ethics/IRB Database

RED is a complete, web-based solution for research ethics/IRB application processing, handling both committee administrator tasks and management information.

Online Form Framework

The On-Line Form Framework uses the power of the internet to provide smart forms that are easy to complete, secure, and exchangeable with colleagues or other systems.

ReDA - Research Management Software

ReDA is a dedicated solution to assist in the portfolio management of research projects and clinical trials.

Tissue Auditor

Professional software designed specifically for the needs of laboratories and tissue banks to meet EU and UK regulatory requirements and the Human Tissue Act.

 

Infonetica Products - Training

UK R&D and Ethics Online Application Process

Having designed and implemented the online NRES ethical review form and the R&D approval form now in place across the UK, Infonetica's understanding of their functionality is second to none.

Online GCP Certification

The online course presents a flexible and cost effective learning opportunity which sidesteps the time and cost issues of classroom based training.

IRAS Training Course

Infonetica are now offering a half-day training session providing guidance and hands-on practice in the use of the new Integrated Research Application System (IRAS).

Company News



16 Jun 2009
Infonetica Contribute to Improving the UK Clinical Research Environment
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)
05 Jun 2009
Infonetica become Microsoft Gold Partners
Infonetica have recently been awarded the staus of Microsoft Gold Partner
27 May 2009
Infonetica chosen to Provide Victoria, Australia Ethics Software
Infonetica have recently been selected and have signed a contract to provide clinical research ethics software to the Department of Human Services for Victoria in Australia.
16 Mar 2009
IRAS Reduces burden of Clinical Research Governance
From 9 March 2009 all the data required to make an application to the MHRA for authorisation of a clinical trial of an Investigational Medicinal Product (IMP) can be completed within the Integrated Research Application System (IRAS) http://www.myresearchproject.org.uk - which is based on the Infonetica Online Form Framework.
02 Feb 2009
IRAS cited in Article
The IRAS system which is based on Infonetica's technology platform is cited in a web article: The calls to cut the red tape that ties up clinical trials in Europe grow louder and louder... Now Europe's legislators are listening hard, and the red tape is beginning to fray... The regulators' single application and - in the UK - the integrated research application system (IRAS) for NHS studies should soon begin to make that purpose clear again.
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