Integrated Technology
Our Laboratory Information System (LIMS) was imlemented and maintained to ensure the security, accuracy, and reliability of patient and testing data.
Advanced Fully Automated Integrated Laboratory Information Management System & IT solutions
The Laboratory Information System (LIMS) are established and maintained that patient and testing data are secure, accurate and reliable. Electronic barcoding for identification of patients, specimens and laboratory testing is used to establish identification and link specimens and tests to a patient throughout the entire testing process including test ordering, specimen collection, analysis and test result reporting. The laboratory controls how patient and laboratory information is received, accessed, transmitted, and stored in both paper-based and electronic information systems.
Fully laboratory automation Solutions:
- Accelerate diagnosis – Deliver timely and consistent lab services Gain process efficiency
- Pre-analytical sorting Manage large sample peaks with high-throughput instrument connectivity options
- Provide predictable TAT for time-critical results analysis
- Extend the test menu capability from a single tube Transform your lab results with advanced IT technologies
- Interface to web portal and remote lab report printers across the laboratory chain for easy patient access Mobile applications
Laboratory Equipment & Technologies
We use CE certified medical Equipment and devices in Europe CE Certified
CE marking is the medical device manufacturer’s claim that a product meets the essential requirements of all relevant European Medical Device Directives. The Directives outline the safety and performance requirements for medical devices in the European Union (EU). The CE mark is a legal requirement to place a device on the market in the EU.
We use FDA approved medical equipment and devices for analysis FDA Approved
The FDA generally classifies medical devices based on the risks associated with the device and by evaluating the amount of regulation that provides a reasonable assurance of the device’s safety and effectiveness.
