Electronic data capture for clinical studies - eCRF Ready

CoLAB Trials

Portugal

Service ID:

EP367S2
Service description

Data quality, speed and ease of data collection, ability to monitor, trace and audit trail with improved regulatory compliance are key for the digital transformation of the data collection process in clinical studies. CoLAB TRIALS has in-house expertise on developing eletronic Case Report Forms (eCRF), enabling higher data quality and a more efficient and standardized process of collecting scientific and clinical evidence. This service is directed to EIC Transition and EIC Accelerator, innovators that will perform clinical studies and clinical trials with health products/services/methods, ex: Medical Devices (including SaMD and IVD), New Approach Methodologies (NAMs including Biomarkers), and Medicinal products (including Pharmaceuticals and Advanced Therapy Medicinal Products). This service will be designed to meet the specific needs of health innovators. The goal of the service is to deliver a user-friendly tool for the collection of appropriate and robust scientific and clinical evidence during clinical studies, aligned with the ethical guidelines and regulatory requirements (Good Clinical Practices, CTR, MDR, IVDR, GDPR). The service of electronic data capture includes: eCRF development, data collection workflow and parametrization, user roles definition, development of rules specific to the clinical study/trial, data maintenance, audit trail. In the end of the service, EIC beneficiaries and innovators will be able to access a user-friendly and GDPR compliant tool for tailored data collection during the conduct of their clinical studies/trials.

Sector
Biotechnology;Health and medical care;Pharmaceuticals
Biotechnology
Digital and Information communication technology
Technology Readiness Level
TRL 5 – Technology validated in relevant environment
TRL 6 – Technology demonstrated in relevant environment
TRL 7 – System prototype demonstration in operational environment
TRL 8 – System complete and qualified
TRL 9 – Actual system proven in operational environment
Financial requirements

The price of electronic data capture depends on the number of users and months of use, with prices starting from 10,000.

Disclaimer related to service

Each requested service will be specific to the clinical protocol and its associated rules of data collection. Meetings to exchange and discuss rules and parametrization might be necessary to deliver the tailored service. The service will be delivered considering the EU regulatory landscape. The duration of the service varies according to its complexity.

i

Are you in doubt if this is the right service for you, or do you want to get more information about the service? Get in touch with the EIC Partner providing this service through this query form!

i

Is this the service you are looking for? If so, you can apply to the service through EIC ACCESS+! Eligible applicants can also get co-funding through the EIC ACCESS+ initiative. Find out more on the project webiste.

Receive up to €60,000 in grants, covering up to 50% of the costs, to access specialised services from the EIC Service Catalogue. Learn more on the EIC ACCESS+ website.