100+ Universities institutions streamline their research processes with Infonetica
Empowering Healthcare Research
Our software has been supporting organisations across the globe since 2003.
Today, the NHS, Clinical Trials Ontario, and the 30+ other academic institutions ensure their research lifecycle is efficient and compliant through our software.
Our mission is to Empower Research to Advance Lives
Research is the engine of progress, driving innovations that transform lives and solve global challenges.
At Infonetica, we're dedicated to empowering healthcare institutions in their quest for medical breakthroughs and improved patient outcomes through our innovative software and unwavering support.
Our commitment is rooted in five key principles:
1. Advancing Human Knowledge: We accelerate clinical research across all specialties, from pioneering gene therapies to revolutionising mental health treatments.
2. Fostering Collaboration: We dissolve barriers between medical disciplines, connecting researchers, clinicians, and data scientists to catalyse ground-breaking medical innovations.
3. Ensuring Ethical Standards: We champion research integrity and patient protection, developing state-of-the-art tools for secure data management and stringent protocol adherence.
4. Democratizing Access: We level the playing field, ensuring that community hospitals and world-renowned medical centres alike can access cutting-edge research tools and methodologies.
5. Driving Societal Impact: We continuously innovate to create efficiencies in the research lifecycle, and drive societal change faster.
Let's take a look at how that looks in practice.
Clinical Trials Ontario saved $18M to the public system
The Challenge:
- Need for a scalable solution to drive efficiencies across their 4600+ active clinical trials across Canada.
The outcome:
- Single workflow that allows 19 different ethics boards to co-exist in the same system.
- Efficiencies and reduction in red-tape leading to an estimated $18 million in cost savings to the public system.
- A "time to Centre Initial Application approval that is significantly lower now than if sites submitted to their local Research Ethics Board for approval." - Scott Tomlinson, CTO Stream Manager
"Clinical trials have become more complex and having a system where users from both the applicant and REB side can collaborate on an application is a definite plus.
The system is inherently user-friendly and training new users such as REB Staff and REB committee members can be done easily."
The system is inherently user-friendly and training new users such as REB Staff and REB committee members can be done easily."
Aurora de Borja, MD, BSc.
Research Ethics Manager
NHS Research Scotland saved 36 days across 12 Health Boards
The Challenge:
- Difficulty in tracking clinical trial KPIs
- Challenges around real-time monitoring to identify problems in trial delivery
- Difficulty in making strategic and evidence-based decisions
- Delays in setting up multi-site clinical trials across Health Boards
The outcome:
- Smarter allocation of government budgets.
- 36 days a month across all Health Boards through centralised data administration.
- Accelerated approval and patient recruitment. of over 40,000 trial participants annually.
"With over 15 years of partnership with Infonetica, our clinical trial operations powered by ReDA and its advanced insights continues to solidify Scotland as a leading nation for clinical trial success."
Ian Anderson
Research Ethics Manager
