Writers averaged 2.3 reports/year. Teams now generate 300-page regulatory drafts in minutes, cutting writing time by 90%.
A global pharmaceutical leader and maker of Ozempic develops medicines for chronic diseases, facing strict regulatory requirements that demand massive volumes of documentation for every new treatment.
Producing a single clinical study report was a multi-month cycle, with staff writers averaging only 2.3 reports per year while daily delays cost up...
“Claude has helped us cut writing times on CSRs by 90% so we can get documentation directly into human hands for review and approval.”
Pharmaceutical company specializing in diabetes, obesity, and rare blood disorders.
Silos forced teams to manually chase data. Now, AI agents identify adverse events in seconds, eliminating weeks of cross-referencing.
Attorneys juggled fragmented tools to search 50,000 cases. An AI orchestrator now routes queries to sub-agents in a single chat.
Complex regulations outpaced manual review capacity. Lawyers now use custom playbooks to automate compliance checks directly in Word.
Auditors spent five days manually validating files. AI now parses the data against contracts, cutting manual effort by 90%.