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      <text bytes="1606" sha1="rw5hshq6slu40tvtsfov0axypt1a4h9" xml:space="preserve">== Welcome to GxPlex == 

Your shared map through the maze of clinical research regulations.


Whether you're a Study Coordinator double-checking an SAE reporting timeline for a Medical Device trial, a CRA preparing for an audit, or a small sponsor wondering what applies to your trial in a new country, GxPlex is built to help you find your way.

=== What you'll find here ===
GxPlex is a collaborative, wiki-style database of laws, regulations, and guidelines relevant to clinical research — covering international treaties (ICH, ISO, WHO...), EU regulations, and national requirements across Germany, Austria, France, the UK, and the US, with more to come.

Every reference is tagged so you can search and compare by country, research scope (IMP, Medical Devices, IVD...), document type, topic, and more.

=== Getting started ===
# New here? 
#* Head to [[About_GxPlex|About GxPlex]] to understand how it's organized. 
# Curious about the story behind it? 
#* Visit [[The_Project|The Project]] to meet the people who started it. 
# Want to help it grow? 
#* Check out [[Contribute_to_GxPlex|Contribute to GxPlex]] — there's a place for everyone, from occasional contributors to organizations ready to take it further. 


GxPlex only works because people like you bring their knowledge to it. 

Thanks for stopping by — we hope you stay.


== Recent documents ==

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[[Document_Index|View all documents →]]</text>
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