Case Report Form Design
Key to Collecting Quality Reliable Data
We know high quality data is the goal of every sponsor. The key, well-designed Case Report Forms, focused to obtaining the data required for your studies objectives and endpoints. Illingworth believes in providing high quality clinical data management to support your drug development needs, reducing unnecessary delays. We provide bespoke solutions tailored to your requirements and provide real time, faster access to data meaning faster decisions can be made to keep patients as safe as possible.
As we are a smaller CRO we can focus solely on your data requirements, in so doing develop trust with long lasting partnerships.Our size also enables us to offer efficient and flexible clinical data management solutions, providing end to end comprehensive clinical data management solutions from Phase I through to post-marketing trials.Our team of experts are committed to upholding a standardised, process-driven approach. The key to a successful working relationship and part of our customer excellence approach with our clients is being flexible to their requirements. Therefore, our Clinical Lead will work to define specific requirements and expectations to meet the partnership objectives.
Illingworth Research Group can perform a full review process, including:
- EDC and Paper Trial Set-Up & Management
- Innovative EDC and Trial Management System
- Data Management Plan (DMP) development
- Data Management Project Management
- CRF/eCRF design and development
- CRF Annotation & Review
- Database Build & Design
- Data validation specifications
- Edit checks Programming & Testing
- Data processing through double data entry
- Query Management
- Medical Coding
- Safety Data Management & Reconciliation
- Data Export/Transfer
- Real-time data viewing and reporting
Electronic distribution for client review
We provide full collaboration with project management teams and have excellent relationships with site staff. This ensures we can liaise with site staff for them to assist in ensuring optimal CRF design with the support of their site knowledge.
Illingworth’ communication with data management staff is paramount to ensure compliance with internal systems, this is an element where we are supported by an experienced and dedicated provider who we have worked with for many years. Syne Qua Non, an organisation celebrating being named as winners of a Queen’s Award for Innovation in relation to their innovative EDC and Trial Management system.
Production of NCR and bound CRFs
Illingworth are confident we can complete prompt delivery of time critical documents. We have excellent working relationships with printing companies who are familiar with the tight timelines involved in clinical research. These companies will work to meet deadlines without compromising the quality of the finished product.