What are the requirements for your specific business? Will the system be compatible with your existing hardware and software? How user friendly is the interface? These are just a few of the questions you'll need to answer before making a decision to switch to an electronic batch recording system.
Bioanalytical method development (BMD) is the process of designing and optimising analytical methods for the quantitative and qualitative determination of drugs and related metabolites in biological samples.
The term "big data" is being thrown around a lot lately but what does it actually mean, and more importantly, what can it do for manufacturers? Put simply, big data is the collection of large data sets that can be analysed to reveal patterns and trends.
The principles of Bioprocessing 4.0 focuses on the implementation of AI to visualise data is becoming popular with companies looking to focus on predictive analytics. Predictive analytics uses machine learning techniques such as digital twins, or statistical models to make predictions about future .
In-vitro diagnostics regulation (IVDR) is the regulatory framework and compliance assessments that pharmaceutical manufacturers follow to gain approval to bring their device to market. In-vitro diagnostic medical devices are tests used on biological samples to determine a user’s health (i.e.
The new medical device regulation (MDR) was released on 26 June, 2022 and sets new regulations aimed to improve patient safety, innovation and maintaining the UK's competitiveness in the global market.