The purpose of quality is to ensure standards are maintained so that products, services and processes are effective and fit for purpose. Laboratories must maintain high quality standards to provide confidence in

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,

Laboratories are fast-paced environments where accuracy and turnaround time is critical, especially for Quality Control labs. Delivering results and meeting customer expectations is paramount, and where

The Medicines and Healthcare products Regulatory Agency (MHRA) has a responsibility to protect public health by ensuring that medicines and medical devices meet applicable standards of safety, quality and efficacy. Each year, they conduct

Operating a laboratory within regulatory requirements can be a challenge.  The wording of regulations is typically cryptic, and there’s always room for different interpretations.  Audit trails are an important factor for compliance because

From our experience of deploying LIMS systems within multiple facilities, we have compiled this list of the best LIMS features that have given

Process 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,