The adoption of electronic document management processes is becoming essential to product development timelines, business productivity and cost savings. Document management and collaboration technologies have made essential and significant advances in helping life sciences companies bring safe drugs and medical devices to market.
Regulatory compliance is a core requirement – ECLINSO products and solutions have been developed to reflect the diverse needs of managing clinical trial enterprise content, helping to improve timely regulatory reporting and minimize the risk of non-compliance.
ECLINSO offers three flexible solutions designed to promote and support collaboration and ease of exchange of confidential data across partner, technological and geographic boundaries.
ECLINSO provides various solution options based on requirements:
- trialeTMF based on Sharepoint
- trialXchange based on Alfresco
- Carizma QM