Superior Clinical Trial Data Management System

Clinical trials involve vast amounts of data and many patients. Reading numerous hand scribbled notes and indecipherable handwriting create confusion. Also, entering data manually can be time consuming and mentally exhausting. Sometimes, a small change in spelling for a name can cause chaos. Many consider using automated systems is a way of policing them and suppose it finds ways for them to work more. This is untrue in most cases because the intention is to reduce the manual tasks to a minimum and assist with inputting data quickly.

The optimal solution to data management in clinical research is a CDMS or Clinical Data Management System. The data collated through these systems will ensure faster drug discovery and shorten time-to-market significantly. The future of clinical trial data management that we see will be more automated with greater use of ‘artificial intelligence’ and ‘machine learning’ to sift data and identify patterns and trends from patients and trials. Big data and these will help speed-up the drug development process.

Top 3 benefits of our clinical trial data management system: Data repository at another level

Strict compliance with defined local and global standards is facilitated

One system for a holistic picture with statistical analysis and reporting key performance indicators

Highly professional and top quality study submission packages.

Significantly lower operations cost for IT and business.

Creating reports is simplified and quick.

Consistent automated data collection prevents user bias or other variables that could manipulate outcomes.

Ensure compliance can be hard-coated

Electronic records control: Our clinical trial data management system accurately reproduces the electronic documents. A complete audit trail of their dates and metadata is maintained.

Accurate sequencing of steps or transactions: a defined security hierarchy can control the object’s life cycle, data access, and system functionality.

Procedural controls: our system performs revisions and traces user who made the changes. Additionally, the system enable electronic signatures when the transaction/ operation occurs.

Speeds-up clinical trials, submissions, and drug launch turn-around time

Accelerates the creation of reports by quickly collating information from multiple investigators, doctors, locations, or clinics.

Sharing and reviewing clinical trial data becomes streamlined and quicker leading to lower time-to-market considerably.

Conclusion

At Qualitas Infotech, we are a customer-centric group of people looking to match our clients’ expectations and ensuring all their compliance requirements are implemented. Our dedicated team takes data management in clinical trials to another level which ensures return on investments for each organization.