Pharma companies must start to rethink their way of authoring regulatory documents to improve quality, enhance writing efficiencies and increase accessibility to content, thus optimising the condition for keeping regulatory documents updated and fully aligned across health agencies. At BASE, we recommend that you transform narrative formats into structured content, by leveraging AI and ML to achieve a smooth process.
In this whitepaper, Badr Fathi and Thomas Røhme suggest an efficient approach to transform regulatory documents into structured content.
