The client came to NEKLO as they saw the need for a custom software solution development providing:
- Digitalized clinical development to help reduce medicine time-to-market by parallelization of multiple steps and automating of complex data management;
- Processing of large amounts of clinical trials data;
- Providing 100% security for the lab data uploaded and stored.
The NEKLO team delivered a user-centric, workflow-driven clinical trial management system (CTMS) allowing full data transparency on each stage of the clinical research
Some of the functionality we added include:
- Data integrity, quality and security when transferring databases, developed in compliance with HIPAA; effective protocol automation in accordance with the industry rules and standards;
- User-centric data access and permission control;
- Organizing users into groups and projects based on healthcare research subjects;
- Availability across multiple platforms.