Data entry for Case Report Form (CRF)

The management of clinical study data is an essential process to ensure the reliability of the obtained results, and efficiency in sharing this information is a crucial factor for the success of the clinical study.

The Data Entry service provides specialised support in recording the clinical study data in the Sponsor's Case Report Form (CRF), ensuring the accuracy and integrity of the collected information. Additionally, the service monitors the queries that may arise throughout the study, ensuring deadlines are met. This service is carried out by a specialised team dedicated to delivering the Data Entry service.

By offering a Data Entry service, we aim to streamline the data recording process, facilitating its sharing among the involved parties, thus promoting the efficiency of the clinical study.

If you need Data Entry support, please click on request service.

What will you have access to when requesting this service?

Guarantee of accuracy and integrity of the data collected

Compliance with timelines defined

Required documentation

In order to provide the Data Entry service, the following documents must be submitted:

Clinical study protocol
CRF guidelines

Benefits of the service

Efficiency in information sharing

Data transmission between Promoters/CROs and CRSs streamlined, ensuring that established deadlines are met.

Data Accuracy and Integrity

Guarantee that the data is accurately recorded, maintaining integrity for the validation of clinical study results

Simplification of the process

Reduction of the time spent on data entry, allowing resources to focus on higher value-added activities

For this service, Portugal Clinical Studies collaborates with the following companies: