Advancements in technology have allowed the availability and delivery of software to be quicker, more secure and more reliable. If you’re still using on-premise LIMS, here are a few reasons why you should consider switching to SaaS LIMS.
SaaS vs On-premise – Why Now is the Time to Consider a SaaS LIMS
by Sophie Blackburn posted in LIMS, Data Management, Process Improvement, best practices, process mapping, deployment projects, Laboratory Efficiency, Laboratory Management, Tips4 Reasons Why You Don't Have LIMS and Tips to Overcome Them
by Sophie Blackburn posted in LIMS, Data Management, Process Improvement, best practices, process mapping, deployment projects, Laboratory Efficiency, Laboratory Management, TipsLaboratory information management systems (LIMS) are known to deliver substantial efficiencies to laboratory operations. From sample management, data comparison and reporting, LIMS can transform the most time-consuming, mundane and critical tasks to simple, easy-to-complete tasks within a click of a button. So, why doesn’t every lab have a LIMS?
LabHQ's Best Features for Pharma
by Sophie Blackburn posted in LIMS, Data Management, Process Improvement, best practices, process mapping, deployment projects, Laboratory Efficiency, Laboratory Management, TipsThe pharmaceutical industry is highly regulated to ensure that the quality, efficacy and safety of medicines delivered to patients is maintained. When pharma companies
What to Do When Your LIMS is No Longer Supported
by Theresa Webster posted in LIMS, Data Management, Process Improvement, best practices, process mapping, deployment projects, Laboratory Efficiency, Laboratory Management, TipsAs a laboratory that has already made the leap from paper to LIMS, moving away from LIMS would be a step backwards, and certainly wouldn’t be the favourable option if your LIMS is no longer supported. What do you do when your LIMS supplier has discontinued service? In this blog, we go through the key areas to consider, so you don’t have to roll back to paper-based systems.
Is Your LIMS Good Enough? Where LIMS Adds the Most Value for Labs
by Theresa Webster posted in LIMS, Data Management, Data Integrity, Process Improvement, process mapping, QC Laboratory Data Management, Quality
When you’re working in a fast-paced environment such as a laboratory, you might not have the time to implement improved ways of working. You may be using an existing LIMS, and are used to the workarounds and quirks of the system.
I Know I Need LIMS But What Do I Do Now?
by Phil Saunders posted in LIMS, Data Management, Project Management, Process Improvement, LabHQ, process mapping, QC Laboratory Data Management, Quality, deployment projects
4 Signs Your Lab Has Outgrown Your LIMS
by Theresa Webster posted in LIMS, Data Management, Data Integrity, Process Improvement, process mapping, QC Laboratory Data Management, QualityMany laboratories introduce LIMS to help with sample data management and reporting. Some labs will have used the same system for 12 years without upgrades, and other labs will
The Best LIMS Features for Improving Laboratory Productivity
by Theresa Webster posted in LIMS, Project Management, Process Improvement, process mappingFrom our experience of deploying LIMS systems within multiple facilities, we have compiled this list of the best LIMS features that have given
5 Steps to Successful Process Mapping
by Vanessa Ford posted in LIMS, Project Management, Process Improvement, process mappingProcess mapping involves a step by step walk through of existing (or proposed) activities considering inputs, outputs, decisions and possible sub processes on which the area of interest may be dependant. As such, process mapping is not only important for determining the scope of a LIMS project,
Return on Investment: Beyond the Regulatory Benefits of LIMS in a QC Lab
by Andy Mooney posted in LIMS, Data Management, Client Expectations, Data Integrity, MHRA, process mapping, Return on Investment,Overheard in the ABC Pharmaceuticals QC lab, "He understands the regulatory benefits of LIMS, but my boss also wants to see a tangible return on investment. Help!"
A major driver for implementing LIMS in regulated industries is the increasing focus of the MHRA, FDA & HPRA on the hot topic of data integrity. Failure to present a quality system that meets the requirements reflected in the ALCOA acronym ( data must be attributable, legible (permanent), contemporaneous, original and accurate) could lead to a loss of licence and result in a devastating impact on revenue.