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 offers solid experience in successfully developing viable systems in partnership with the public sector and other organisations-a company small enough to be flexible and responsive but with excellent technical know-how  and a strong team for sustainability and reliability.

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

Online GCP Certification

Our Online GCP courses present a flexible and cost effective learning opportunity which sidesteps the time and cost issues of classroom based training. Choose from the GCP Practical Implementation course or the Introductory course on the Principles of Good Clinical Practice-different language versions available

IRAS Training Course

Infonetica now offer face-to-face training in the use of the new Integrated Research Application System (IRAS). Up-to the-minute practical guidance on all that IRAS has to offer.

Company News



16 May 2013
Are You Prepared For The FDAs Upcoming Sunshine Act?
The US FDA has measures in the pipeline that aim to ensure clinical trials are carried out ethically and for the right reasons. Under the proposals payments to physicians for participation in trials would become more transparent.
16 May 2013
2013 Annual NHS R&D Management Forum Conference
This year we are the Headline Sponsor at the NHS R&D Management Forum Conference.
12 Nov 2012
Pharmacovigilance Training

Pharmacovigilance Training & Drug Safety

Pharmacovigilance training and drug safety were developed to prevent another Thalidomide disaster. The present day approach to drug safety and adverse event reporting started with the Thalidomide disaster. This drug was prescribed in many countries around the world, but never in the US, to alleviate morning sickness in pregnant women. Thalidomide is a teratogen and caused horrific birth abnormalities. However these were not reported as adverse events since no such system existed at the time, and so it took a few years before people realized what was happening. This led to the introduction of adverse event reporting and the creation of Pharmacovigilance training.
24 Oct 2012
ReDA Open Day Invitation
You and your team are invited to our upcoming open day. This year we are holding two open days to make it easier for you to attend. The day will give you an opportunity to network with other ReDA users, find out about the latest product developments and, importantly, help us to ensure that ReDA continues to deliver what you need.
13 Aug 2012
Whitehall Training
Infonetica are proud to have launched the Whitehall Training website! We offer flexible and cost-effective courses on GCP, Pharmacoviglance and GDP. Students develop their skills and earn CPD points with industry-recognised compliance training. Trainers and administrators save time by assigning and managing licences with our easy-to-use admin system. All courses are written by recognised experts and accredited by leading academic institutions.
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