EDITORIAL
Welcome to the CDMO expertise blog!
It is with great pleasure that we welcome you to this CDMO expertise blog.
Through the meetings and exchanges that we have been able to make in the pharmaceutical universe, we have been regularly in a position to answer questions concerning, for example, the practices of the pharmaceutical subcontractors, the optimization of the production capacity, the key success factors of a subcontracting project but also more up-to-date topics such as serialization, the 2016 version of ISO 13485, the galenic forms of the future … Naturally, it seemed to us that all these queries could find answers on a single blog around the pharmaceutical expertise of a CDMO.
Share and innovate together in the pharmaceutical industry
As a CDMO, our main objective is to share our knowledge and skills of the pharmaceutical world on a single platform. A pedagogical vocation, this blog is a place of discussion on subjects that animate us jointly and daily in our missions.
This is why we want to start a dialogue with you around all the questions you ask yourself and to discuss our common issues.
Each week the team will share with you various posts in order to accompany you on a daily basis, to help you and feed you with topics from the pharmaceutical world. Because there are more ideas in two heads than in one, we work as a team to provide you with quality content but do not hesitate if you have topics that you want us to address.
Enjoy your visit!
