Data integrity being a major concern in the regulated pharmaceutical industry, as it is a critical part of the FDA’s mission to ensure the safety, efficacy and quality of human and veterinary drugs, biological products and medical devices, scientific laboratories are looking for ways to maximize their results output from Empower and ideally utilize this one system as their only solution for chromatographic results.

Master data is the core set of information which provides the context in which the LIMS operates, and is a critical part of any deployment. Building the right Master Data architecture will improve workflows, allow for better maintainability over the long term, avoid common pitfalls, and create a data structure which will allow your laboratory to function more smoothly.

When laboratories consider modernizing their technology and infrastructure, they often overlook evaluation of their business processes such as developing a lab informatics roadmap. With today’s increasing complexity in research it is imperative that your informatics strategy incorporate a holistic approach to enhancing your business processes, data flow, and technology solutions.

Many scientific R&D organizations are interested in applying machine learning (ML) and advanced analytics (generally “AI/ML”) but are intimidated by lack of clarity on how to get started, the apparent complexity, or how to best achieve practical outcomes.

Are you aware of the many different modules available on Thermo Fisher Scientific’s SampleManager LIMS™ and their potential use for your system? Learn from the experts at Astrix about how these solutions can help you get the most value from your SampleManager LIMS.

With comprehensive reporting, monitoring, managing and analysis capabilities, STARLIMS has a wide range of configurable features to maximize performance and value to transform your laboratory workflow.

Validating a LIMS with the many configuration and integration options that are available for LabVantage requires significant project planning and team coordination to execute successfully. 

With dozens of LIMS vendors now available to choose from, and an increase in specialization in terms of targeted laboratories and increasing demands for cloud-based applications, selecting the best LIMS has become more difficult than ever. 

For large organizations utilizing complex laboratory informatics systems such as LIMS, ELNs, and SDMS, creating a fully integrated data environment is an important key to scientists’ productivity. Too often, however, companies lack an effective methodology to successfully achieve the desired digital continuity across the project lifecycle.

FDA enforcement actions can result in significant consequences. Including data integrity assessments in your organization’s quality management system as part of cGMP audit programs help to ensure compliance with FDA regulations.

IT professionals are often tasked with supporting current infrastructure instead of developing strategic roadmaps. In order to future-proof your lab, an expert third-party informatics vendor can be a valuable partner to your organization.