Regulation, cut down to a size you can read every week.
Global Regulatory Monitor collects the GMP and quality news that regulators publish, and turns it into something you can read once a week. You don't need to work in regulatory affairs. Whether you're in production, quality, research or sales, it's built so the regulatory stories that touch your work are easy to pick up.
Why it exists
There is a lot of regulatory news. FDA, EMA, MFDS and others publish something almost every day, and each item eventually connects to someone's work. Reading all of it, every time, is hard. It isn't obvious where to look, or what to read first.
And regulation feels difficult before you even start. Clause numbers and acronyms get in the way, and before long "regulation" becomes something only the regulatory team looks at. But the people who get cited in an inspection, and the people who fix what was cited, are the ones doing the work on the floor every day.
So this exists. It gathers what is scattered, puts difficult documents into readable language, and keeps a link to the original so you can always check. The hope is that regulation feels a little closer.
How it's made
Public documents from regulators are collected automatically every day, and each Monday morning the week is put together as a brief. Summaries and translations use generative AI; numbers, dates and quoted text are left untouched. Every card links to its source, so you can check whenever you want.
What it holds to
- The source comes first. A summary saves reading time; the judgement is made from the original.
- Facts and interpretation stay apart. What the document says and what the editor adds are separated by colour and position.
- AI-made content says so. Where automatic generation ends is never hidden.
Contact
If you have a question or a suggestion, just let us know. The same goes for anything you find that's wrong.
