Regulatory Intelligence demo
A morning front page of what FDA, EMA, PMDA, NMPA, MHRA and 59 other sources changed, led by what matters most to your products. 1:15
What the demo shows
A regulatory watch solution for regulatory affairs that explains what agency changes mean.
Seven agents check 64 sources every morning, translate, summarize, compare revised documents with the versions they replace and propose the impact per product. Early each morning the front page prints; a regulatory lead signs each High and Medium impact before teams are told.
Transcript
- Regulatory Intelligence tells Regulatory Affairs teams what each agency change means for their products.
- By hand, a change takes seven and a half days to reach its team.
- At five, the agents check 64 sources.
- At 12 past five, the front page prints.
- The lead, an EMA draft with the highest impact on your products.
- Against the 2019 version, two of 11 change paragraphs change your plans.
- A notified body opinion and deliver dose data on three batches.
- The Veltrimab auto-injector filing holds only if the notified body is booked by October 30th.
- Dana signs. Lena and Tom get the exact paragraphs that morning.
- Every change now reaches its team within hours, not a week.
- built on Botminds, agents, data, screens, and governance on one platform.
Transcribed from the film’s narration. Captions are on the player.