It’s that time of year when many life sciences organisations will be reviewing their regulatory information management (RIM) capabilities. This means they’ll be determining what they need to see them through not just the next wave of mandatory submission and reporting requirements (eg under EMA’s implementation of ISO IDMP) – but also a future in which digital process efficiency is the new normal.
So what should some of the key considerations be when surveying what’s on the market, and what does a robust and future-proof RIM capability look like in 2021 and beyond?
Max Kelleher has written a helpful ebook to guide you through the selection process.
