Smarter clinical research data systems, built around your study.
Whether you need expert advice, a new research database or automated IMP-management tools, AGC DATA can help you develop practical, reliable and inspection-ready infrastructure tailored to your study.
Supporting clinical research teams and organisations across the UK and internationally.
AGC DATA
AGC DATA helps clinical research teams design, develop and manage reliable data systems through database development, automation and system integration. We turn complex study requirements into practical tools that make research data easier to collect, manage and trust.
CTIMP Database Development and IMP Management
CRISPNet is an IMP-management tool developed by AGC DATA for Clinical Trials of Investigational Medicinal Products. It integrates with electronic data capture systems such as REDCap to support and automate critical trial workflows, including treatment allocation, IMP allocation, inventory monitoring, drug accountability and emergency unblinding.
CRISPNet is designed to strengthen data integrity, traceability and oversight through automated workflows, role-based access, data-quality controls and complete audit trails. Each implementation is configured around the study protocol, sponsor requirements and agreed validation approach, helping research and pharmacy teams manage IMP processes securely and efficiently.
Non-CTIMP Research Database Development
We design and implement electronic data capture systems tailored to observational studies, registries, laboratory projects, tissue banks and other non-CTIMP research. From protocol review to first participant enrolment, we translate your requirements into a structured, practical and user-friendly database.
Our systems can include automated validation, participant and visit tracking, data-quality dashboards, surveys, reporting tools, sample management and ongoing technical support. Each database is developed around the study’s requirements and the responsibilities of the organisations involved.
Draw on practical experience developing dependable data systems for clinical research. AGC DATA specialises in building structured, user-friendly databases that support consistent, reliable data collection from the beginning of your study.
Book a free consultation to discuss your study’s needs.
Data Management Consultation
How we can support your project
1. Discovery and Consultation
Whether you are starting from the beginning or trying to resolve problems within an existing project, the free discovery call gives us an opportunity to understand your study and current challenges.
We can discuss your protocol, database requirements, suitable tools, potential risks and the likely development process. Where further work is appropriate, we can also provide an initial indication of timescale and cost.
There is no obligation to continue after the call.
2. Database Design and Development
We design, configure and test an electronic data capture system tailored to your protocol. This can include blinded workflows, randomisation, multi-site coordination, complex visit schedules, automated validation, live dashboards, participant surveys and complete audit trails.
Testing, documentation and validation activities are agreed according to the requirements and risks of the study.
3. CRISPNet IMP Management Integration
Add automated IMP-management workflows to your study database.
Where your protocol requires randomisation, IMP allocation and full drug accountability, CRISPNet can be integrated with your study database to support treatment allocation, maintenance of blinding, dosing workflows, pack allocation, inventory monitoring, expiry management, emergency unblinding and traceable audit records.
Your project may require one stage or the complete development pathway. Each stage builds on the previous one, allowing you to choose the level of support your study needs.
”Jordan has provided valuable data management and technical support to our research, translating complex project requirements into practical and effective systems. He has been responsive, solutions-focused and able to understand both the technical and operational needs of the research team. The infrastructure and processes he has developed have helped improve the efficiency, consistency and overall management of our research data.”
- Dr Jacqueline Maybin, BSc, MBChB, PhD, MRCOG
“Jordan designed and developed an attractive, intuitive and easy-to-use set of data collection tools and an accompanying research database for our project. He took the time to understand our requirements and translated them into a practical system that made the collection, organisation and management of our research data straightforward for the team. The finished database was well structured, user-friendly and tailored to the needs of the project.”
- Sue Spencer, BSc (Hons), RGN
”Jordan has been instrumental for creating, administrating, and maintaining our study’s RedCAP database with bespoke data collection tools, with a focus on our needs and rapid turnaround. Jordan’s work seamlessly integrated different data sources and records, which has allowed us to easily identify and extract relevant research data from thousands of data points. Without Jordan’s help we would not be able to streamline our participant recruitment, data collection and analysis so effectively”
- Professor Erin Greaves, PhD
”Jordan supported the WERF EPHect initiative by developing a standardised digital version of the EPHect surgical form for use by research teams internationally. He translated a detailed clinical research form into a structured and practical data collection system, helping to support consistent collection of surgical data across different projects and locations. Jordan also provided valuable administrative and organisational support to the wider initiative.”
- Lone Hummelshoj, EPHect Programme Manager, World Endometriosis Research Foundation
Frequently asked questions
Will our organisation retain ownership of its data?
Yes. Your organisation retains ownership and control of its research data. AGC DATA only accesses or processes information where necessary to provide the agreed services. Data access, confidentiality and processing responsibilities are documented as part of the project agreement, and a mutual non-disclosure agreement can be put in place before detailed study information is shared.
Can AGC DATA support GDPR and HIPAA requirements?
Yes. Systems can be designed and configured to support applicable data-protection and information-security requirements, including UK GDPR, EU GDPR and HIPAA-related controls where required.
The specific approach will depend on the study, participating organisations, hosting arrangements, system providers and allocation of responsibilities. Relevant controls may include regional hosting, role-based permissions, multi-factor authentication, audit trails, controlled integrations and documented data-processing arrangements.
Who does AGC DATA work with?
We work with clinical research teams across a range of roles, including principal investigators, trial managers, data managers, pharmacists, research nurses, laboratory teams, statisticians, analysts and information-governance professionals.
Whether you are planning a new study, improving an existing database or resolving problems within an active project, AGC DATA can provide practical support.
What does the AGC DATA development process involve?
Our process is flexible and can include one or more of the following stages:
Discovery and consultation – We discuss your study, existing systems and operational requirements.
Database development – We design, configure, test and document an electronic data capture system tailored to your protocol.
CRISPNet integration – For CTIMPs, we can integrate IMP-management workflows covering allocation, accountability, dosing, inventory monitoring and emergency unblinding.
Is the discovery call really free?
Yes. The initial call gives you an opportunity to discuss your project, ask questions and receive an honest assessment of the most appropriate next steps.
Where AGC DATA is a suitable fit, we will outline a potential approach. There is no pressure or obligation to continue.
What does AGC DATA do?
AGC DATA designs and supports data systems for clinical research.
Our services include electronic data capture, REDCap database development, workflow automation, participant and sample tracking, reporting tools and specialist IMP-management infrastructure for CTIMPs.
From early study planning to close-out, we make research data easier to collect, manage and trust.
Discuss your project
Whether you are planning a new study, reviewing an existing database or trying to solve a difficult data-management problem, contact AGC DATA to discuss how we may be able to help.