Have you ever taken on a project that is large and overwhelming that you didn’t know where to start? It can feel like everything is blurry, and you’re looking for your glasses to bring your sight into focus. Deploying a LIMS can often feel like this, and risk assessments can help you bring the project to focus.
Laboratories look to gain ISO 17025 accreditation as recognition of their competence and abilities, to help them improve and monitor their operational processes, and to satisfy customer requirements. At the end of 2017, an update to the ISO 17025 standard was issued. In this blog, we give you
Laboratory Managers are frequently overwhelmed with the amount of work they need to complete. Especially in a Quality Control laboratory, where turnaround times are crucial, routine operations continually takes priority, but what if
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.
Many 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
"I’ve got a great idea that will generate laboratory efficiencies. How do I get it approved by the boss?"
Organisations are increasingly looking to Departmental Managers for ideas that will generate cost savings via process efficiencies. Take a look
Validating LIMS is a fundamental requirement for GMP compliance. Where LIMS is used to store and process GMP data, it is imperative that
What are they
User Requirements are a list of activities and functions which users of a software system would like to use or need to use in order
The concept of cloud computing has actually been around since the 1960s, and it wasn’t until 2006 that it started to gain traction in industry. In contrast to the cloud,