Achieving regulatory excellence depends on a combination of optimisation processes, effective global systems, high data quality, and enhanced affiliate collaboration. However, transforming information management at…
These days, clinical trials are in the news pretty much daily. Whether successful or not, they can impact not only the perception of a pharmaceutical…
As well as exposing companies to non-compliance, inefficiency and delays, a manually-maintained pharmacovigilance system master file (PSMF) limits visibility and transparency. Christian Schmitz-Moormann, a senior…
A multimode plate reader is a device used to read and analyse culture or test plates in biological or chemical experiments, it can detect two…
Decentralised clinical trials (DCTs) are not new, though their popularity and utilisation has grown since the COVID-19 pandemic. DCTs are enabled by and mutually reinforce…
Neo4j’s Alexander Jarasch explains how to get the best from ChatGPT-like tools, while safeguarding intellectual property ChatGPT has delivered a natural language understanding (NLU) interface…
Rituals play a significant role in human lives, offering a sense of structure, routine, and meaning to our daily actions. While rituals are commonly associated…
Adnan Jamil of Deloitte sets out specific recommendations and emerging leading practices as Life Sciences organisations assess what’s needed from next-generation regulatory information management (RIM)…
Direct pharma-patient engagement used to be considered largely a “nice to have,” and was, at best, a rare occurrence at specific times during the pharmaceutical…
Pharmaceutical companies are placing greater emphasis on consistent and unified data flow throughout their operations, creating a flow of broader data and insights between functions….
