All the resources for funding are available in our Ségur section for digital equipment.

For your application to be complete, you need to include several credentials and documents.

The list of documents and credentials needed is detailed in the Application form (download it below). You will need to send and application for each product you wish to label.

You must return your application form with all the supporting material by email AND via postal services:

1. the complete application form needs to be sent by mail to:

   Agence du numérique en santé (ANS)
   Labellisation logiciel Maisons et Centres de Santé
   9, rue Georges Pitard
   75015 Paris

2. follow up with sending digital versions (PDF scans) of the agreement and its annexes, in two copies, signed and completed to:

   labellisation.msp@esante.gouv.fr

When your software gets the label attribution, the successful candidate will receive by email the visual elements you will need to communicate about it.

The editor of the solution (or the solution range) will receive the label after signing the agreement with the ANS. They will be able to use the label on commercial publications, technical documents, with no particular restriction on the type of format used (paper, Internet, intranet, etc.) 
The recipient must mention the level of the label (1 or 2) they obtained. These specifications are set out in the Functional referential (in our Documentation section)

There are several levels of requirements for a module’s integration into the Hospital Information System. 

The main requirements set out by the referential are: 

• Interfacing, control, security guidelines; 
• Prescription process requirements; 
• National prescription thesaurus integration requirements; 
• Requirements regarding medico-economic and decision processes; 
• Guidelines for ergonomics, functions, and notification alerts; 
• Settings function requirements. 

In total, 139 requirements are used to reach the minimal level of security needed for a solution’s integration into the hospital information system.

The current referential (2017) was written with industry experts. It introduces the particular context of this mission and the goals to reach in order to improve safety measures in neonatology and paediatric reanimation. The referential walks you through the fundamental concepts you need to grasp to understand the several requirements and protocols involved with software development for this sector.

Neonatology is a high-risk practice for two main reasons:

• The patients are extremely fragile (premature babies) 
• 50% of the drugs used in the sector have yet to receive a marketing authorisation.

A survey conducted in 2014 evidenced a risk in the prescription process across the sector. The digitalisation of prescription is among the 41 recommendations that the report issued in order to increase safety levels.