Clinevo CTMS

Pros: Excellent CTMS Covering all Study Related Activities
• This system provides the user with any information they want for study/project on real time basis.
• The main goal of our CTMS to create a global system to streamline the clinical trial process, enhance the productivity, Improve client and site relationship.
• The System offers a secure, centralized location for data collection, storage and retrieval.
• It keeps track of a study's financial data, ensuring accurate invoicing for sponsors and proper payments for each site.
• Many research sites and institutions conduct hundreds of clinical trials every year, and a CTMS can help improve the overall efficiency within each trial.

Cons: eLog was not available but it is already in implementation stage now.
It provides functionality for tracking and managing regulatory information across the enterprise, such as amendments, protocol and subject deviations, and more. Additionally, staff credentials can also be tracked within the system.
• Major and Minor protocol deviation can be tracked at study and site level.
• CTMS is connected with eTMF and EDC so the activities which are done in CTMS can be directly captured in the respective section of eTMF and EDC system.

Overall: It is really great experience while implementing the CTMS and also other tools from Clinevo like eTMF, EDC, QMS, TMS and PV database.