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Laboratory Information System (LIS)

Typically, an LIS is composed of several modules that are designed to perform specific tasks. These modules may include specimen processing, result entry, quality control, reporting, and billing. Some LIS systems also offer features such as interfaces to electronic medical records, barcoding, and automated data analysis. LIS systems can be either standalone or integrated with other systems, such as electronic health records (EHRs) or laboratory information management systems (LIMS). Integration with other systems allows for seamless transfer of data between different parts of the laboratory and helps to ensure data accuracy. Overall, an LIS can improve laboratory efficiency, reduce errors, and enhance patient care by providing accurate and timely test results. A Laboratory Information System (LIS) protocol is a set of guidelines and procedures that govern the use of the LIS within a laboratory setting. The purpose of an LIS protocol is to ensure that laboratory data and information are managed and organized in a consistent, accurate, and secure manner. The following are some common elements of an LIS protocol: 1. System Access: The protocol should specify who is authorized to access the LIS, how access is granted, and what level of access each user is allowed. 2. Specimen Management: The protocol should outline the procedures for labeling, tracking, and processing specimens in the LIS. 3. Result Entry: The protocol should provide guidelines for entering and verifying test results in the LIS, including how to handle abnormal results and how to document any changes or corrections made to the data. 4. Quality Control: The protocol should describe the quality control procedures that are in place to ensure accurate and reliable test results, including how to monitor and maintain instrument performance, how to handle quality control samples, and how to troubleshoot issues that arise. 5. Reporting: The protocol should specify the format and content of reports generated by the LIS, as well as the procedures for distributing and archiving these reports. 6. Security: The protocol should outline the security measures that are in place to protect laboratory data and information, including user authentication, data encryption, and backups. 7. Maintenance and Support: The protocol should include procedures for maintaining and troubleshooting the LIS, as well as the protocols for seeking technical support from the vendor. By implementing an LIS protocol, laboratories can ensure that their LIS is being used in a consistent and effective manner, which can help to improve laboratory operations and enhance patient care.

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Laboratory Information Management System (LIMS)

Project Overview * Enable workflow automation which can in turn reduce human error * Centralize access and storage of quality control data * Support compliance efforts * Perform instrument run monitoring * Initiate downstream data analysis * Integrate with instruments or other in-lab systems to improve lab efficiency * Improve quality control and monitoring. * It offers an easy to use and flexible interface for managing jobs and system reporting. * Real time, remote access to progress and results. * Track samples and chain of custody, including barcoding. * Export results in multiple formats. * Schedule and assign tasks and user access * Monitor performance * Receive instant notification of quality errors or concerns. Our flexible, modular approach integrates multiple applications and multiple teams from the lab, field, or office.. Your production data is managed by software designed specifically for different users in different departments. We believe the most efficient way for you to operate your lab is with software and hardware that is specific to the user, connects with a central system, and makes reporting and monitoring easy. When you work with Online LIMS, you get a customized solution that integrates all your devices and systems, helping you automate successfully. Manage Patients Seamlessly manage patient data, demographic details, clinical history, and patient consent, anonymize sensitive patient data, to meet ethical and legal requirements. Patient Portal Enable patients to self-register on the portal, place test requests, associate themselves with physicians, and download test reports as soon as they are released by your laboratory Sample Management Enable users to enter patient data, print bar coded sample labels, associate patient records with samples, place diagnostic test requests, track request status in real-time, download test reports and invoices. Manage Tests Manage tests and their results, validate and authorize test results, automate the calculation of complex test results, and analyze trends based on test results. You can configure flagging sets to automatically flag out-of-specification results and select one or more approves for a test type. Furthermore, you can print labels with barcodes for multiple tests. You can include a QR code on test reports for authentication and an ID to uniquely identify each test report. Follow Regulatory Compliance and laboratory best practices. Access Management Access to the system will be role based so that segregation of responsibility e.g: pathologist, technician, doctor, front office, agent etc, will be maintained. Manage Services and Billing Manage laboratory services, such as test requests, and create catalogs with defined pricing for each service offered by your laboratory that can be varied based on branch and agent. Billing of services can be tallied based on counter. Manage service discount and service reversal MIS Report Our system can generate custom reports for various roles for better management of workflow and increase in efficiency. TAT Analysis Our system gives an option to calculate and monitor TAT of sample at detailed level and TAT of tests at summary level, TAT delay, Delay reason etc. to increase the efficiency of the lab.

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