Rulify tracks FDA, CMS and HHS activity beside fifty state health departments — for providers, medical device makers, digital health and pharmacy teams.
Helping teams from startups to global enterprises stay ahead of regulatory change.
Rules, guidance, enforcement and deadlines from every health regulator you answer to, stacked into a single reviewable feed.
Explore the platformHealthcare compliance runs on layered agencies, fifty state registers, and a surveyor who will ask how you kept up.
Rulify does the six jobs a healthcare compliance program needs done, continuously.
Device, drug and biologics rulemaking, draft and final guidance, and enforcement activity, matched to your product lines.
Payment rules, coverage decisions and program requirements, mapped to the provider types and programs you bill under.
Privacy and security rule changes, OCR guidance and enforcement trends, sorted into what your program must update.
Licensing, telehealth and facility requirements across all fifty state health registers, on one profile.
Every compliance deadline extracted from the rule text and phased exactly the way the regulation phases it.
A record of every regulatory change reviewed: when it surfaced, who assessed it, and what actions followed.
Healthcare regulatory intelligence as a working routine — matched, summarised and assigned from the first day.
A draft guidance lands. Rulify matches it to your devices or programs, summarises it, and creates review tasks with the comment deadline attached.
Answer surveyors and auditors with a record: every relevant regulatory change, when it surfaced, who reviewed it, and what was done.
Pull the licensing, telehealth and facility requirements for every state a new service enters — before launch.
Tell Rulify what your business needs to watch. We track the relevant sources and alert you the moment something moves.