RIP Responsibilities

𝐃𝐨 𝐲𝐨𝐮 𝐤𝐧𝐨𝐰 𝐰𝐡𝐚𝐭 𝐑𝐈𝐏 𝐫𝐞𝐚𝐥𝐥𝐲 𝐦𝐞𝐚𝐧𝐬?!

PHAROS blog post

More price negotiations on new expensive drugs in the Netherlands

Evaluation of digital medical technologies in Belgium

Recently, the Belgian Healthcare Knowledge Center (KCE) published a report on the evaluation of digital medical technologies, to which Sven and Frank participated as stakeholders and Domien contributed as an external validator.

Regulatory Compliance

Many people working in Pharmaceutical or Medtech companies ask us what kind of a consulting agency AxTalis is nowadays. Therefore, we are keen to inform you what you can expect working with us.

Welcome to our team!

We are honoured to be joined by Sabrina Lagniau as Regulatory Affairs Officer.

Merry Christmas!

Dear network,

The AxTalis team wishes you a joyous Christmas and a happy, fulfilling, new year!

AxTalis @ RIZIV

AxTalis at the course “Introduction to Regulatory Affairs” at RIZIV’s.

Welcome to our team!

We are honoured to be joined by Marlies Boeren as Medical & Market Access Manager.

Welcome to our team!

We are honoured to be joined by Wim Neckebroeck as Director Regulatory Affairs.