Key roles of ELN in Laboratories
An electronic laboratory notebook (ELN) is a computerised system that includes tools for creating and storing experimental protocols, results, and research findings on a digital platform. ELNs have been developed for scientists and laboratory analysts working in fields such as chemistry, biology, analytical, in vivo, and clinical research. They play a vital role in […]
How Logilab SDMS Can Be An Effective Instrument Data Management Solution For Your Research Laboratory
If you’re on the fence about what exactly the Logilab Scientific Data Management system can do for your research laboratory, stick around as we deep dive into its powerful instrument data management features and what good they bring to the table. These capabilities are sure to help your lab achieve compliance with various regulations, but […]
How Qualis LIMS Software Can Fit Into Laboratory Data Management Across Various Industry Verticals
In a typical laboratory, the amount of data generated grows over time, increasing storage and processing constraints exponentially. Once the complexity gets to a certain threshold, it becomes a nearly impossible task to manage samples and track data solely through manual efforts. It is at this point that mere spreadsheets fall short, and that’s where […]
The Role Of A LIMS In Modern Laboratories
What do you think is the role of a laboratory information management system (LIMS) in a modern laboratory? Are you considering using a LIMS for your laboratory? Here is some useful information for you. A laboratory brims with data and information. Everything is information in a laboratory. A LIMS, hence, is a software application that […]
Understanding the Need for Regulatory Compliance in Laboratory Informatics Solutions
If you have been a LIMS vendor or are a company that falls under the life sciences field for quite a while now, you probably already know that regulatory compliance goes hand in hand with working in the said field. In fact, many experts that work in labs and other types of research entities that […]
How Logilab ELN can help you Improve the Accuracy & Traceability of your Research Data
The importance of data traceability and accuracy couldn’t be underscored more as far as any kind of research is concerned. It serves as the primary way for studies to be verified not only by the researchers who conducted them but by other third-party investigators, too. In a perfect world, maintaining data traceability and accuracy should […]
On-Premises LIMS Vs SaaS LIMS – A Comparative Analysis
Every modern laboratory in the industry is constantly focusing to enhance its operational efficiency, decrease costs, control regulatory compliance, and improving quality. Apart from this, the rise of Contract Research Organization and R&D externalization strategies in the industry of pharmaceuticals has led to laboratories gathering enormous data from different partners, preceding a significant increase in the complexity […]
Steps involved in finding the perfect SDMS
Before getting into the steps involved in finding the perfect SDMS, it is essential to understand the meaning of SDMS. A scientific data management system (SDMS) acts as a centralized document management system, collecting, cataloguing, and storing data generated by and in a scientific lab. An SDMS is designed to handle unstructured data from data systems like a LIMS or […]
Business Continuity Plan for GxP Compliant Computerised systems
For the availability of computerised systems critical processes, provisions should be made to ensure continuity of support for those processes in the event of a system breakdown (e.g., a manual or alternative system). The time required to bring the alternative arrangements into use should be based on risk appropriate for a particular system and the […]
What is Data Integrity ? Steps to protect the integrity of your data.
Data Integrity Data integrity, an area of increasing priority in today’s laboratory world and “The focus area” when it comes to regulatory compliances such as 21 CFR Part 11 and Eudralex Annex 11. Considering the number of warning letters from USFDA and other such regulatory bodies issued to pharmaceutical and medical device manufacturers across the […]