Post by Allyfe

Mid-size pharma running EU trials, listen up. Every single day your regulatory team does this: 1) Logs into CTIS 2) Takes 15–40 screenshots of approvals, RFIs, ASRs (because there are still zero APIs in 2025) 3) Saves them in a folder called “CTIS_mess_Nov2025” 4) Someone later drags them one-by-one into the eTMF and and prays they’re classified correctly. Hope nothing gets lost before inspection Result? → Weeks of manual work → €100–400 k per study in hidden reconciliation costs → Constant low-grade panic We just solved it. Allyfe now turns every CTIS screenshot (and every scanned legacy PDF) into a perfectly classified, DIA-coded, searchable TMF artifact in < 3 seconds – zero human (but full human oversight, of course). And yes, we already have the “magic email inbox” live: forward the screenshot from your phone, PC → it lands in a secure staging area → one click → everything is filed correctly while you drink your coffee. This is not science fiction. It’s running today. The future of sponsor-owned, inspection-ready TMFs just arrived. #ClinicalTrials #eTMF #CTIS #RegulatoryAffairs #Pharma