In clinical labs, a persistent need for lab information management software exists. However, up until recently most companies would purchase many different types of software systems and then customize it to meet the laboratory’s needs. In order to customize the software, skilled scientists capable of managing software implementation and customization were needed. This practice can be problematic, however, as it removes scientists from the discovery process to manage lab infrastructure issues and software integration problems. Furthermore, data sharing between colleagues within clinical labs and other collaborators across diverse industry environments to accelerate findings within the discipline is vital, reported Fierce Biotech.
The rapid pace of discovery in NGS, omics and clinical labs requires lab data management technology to integrate seamlessly from multiple sources. Additionally, enabling the sharing of data with remote collaborative teams provides scientists more time to focus on their science, not on software management.
Advancements in sequencing, microarray and qPCR has increased the need for the technology in the lab. Additionally, precision medicine has further accelerated the demand for these technologies. Fierce Biotech states that “this combined with CLIA/CAP requirements for clinical labs has driven processes away from paper based and towards LIMS.”1LIMS securely captures and stores sample data as well as other records related to the staff executing specific test protocols.
Many people wonder what is driving the demand. According to Fierce Biotech, an increased focus on precision medicine as well as advancements in genomic technologies leads to more clinical labs. An increase in the number of clinical labs requires for more testing services. Many labs are opting for LIMS data management solutions instead of paper-based solutions.
Also, physicians continue to seek the most targeted therapies for their patients. Personalized medicine requires fast lab delivery as well as full compliance with patient data safety requirements. Informatics solutions can deliver immediate access to data with “no artificial barriers related to the sources of that data.”1
Pearl IRB is an independent review board with written procedures for efficient review of clinical trials, proper documentation and record retention. If you need support for your current or upcoming clinical trials, contact us today.
1https://www.fiercebiotech.com/sponsored/growing-need-for-data-management-solutions-clinical-labs