mFlow - Medical Forms, Licensing and Organisational Workflows 

Welcome to mFlow - an open-source, flexible pharmaceutical information management system designed with healthcare regulatory frameworks in mind.

mFlow has been developed by the team at The mSupply Foundation - a friendly bunch who aim to create useful, open-source software in order to improve healthcare solutions in low to middle-income countries.

Creating mFlow has been a labour of love — thousands of hours of work. We hope you find it a joy to use, and that it results in your regulatory organisation being able to perform its role accurately, quickly and to a high standard.

mFlow’s development was kindly sponsored by the Australian Government’s Department of Foreign Affairs and Trade.

What can it do? 

mFlow provides a platform to:

• Create application forms
• Manage complex application lifecycle workflows
• Assign roles and permissions to users
• Monitor the status of groups of applications
• Catalogue outcomes of applications

Some examples of regulatory frameworks where mFlow is currently being used:

• New Drug Registrations
• Pharmaceutical Company Licensing
• Medicine Import / Export Permits

mFlow’s flexibility means that it can be used in a wide range of situations. For clarity, this guide focuses on its intended use in healthcare regulatory environments. Suggestions for use of mFlow in other situations can be found in the Uses of mFlow chapter.