A RIM (Regulatory Information Management) System is a centralized and customizable system that allows you to have all the data and regulatory information of your products in one reliable and concrete place.
Don’t you know how IDMP can affect the way you store your data?
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As Brexit is quickly coming closer, the CMDh has published an updated version of the Practical guidance for procedures related to Brexit for medicinal products for human use approved via MRP/DCP in December 2020.
Asphalion is excited and proud to officially welcome Javier Febrero Alija to its team as Regulatory Information Manager, expert in Data Management and RIMS.
We wish you Happy ‘Xmas, Prosperous New Year and Health for you and your loved ones.
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As a company committed to sustainability, we follow the UN’s 2030 Agenda and its Sustainable Development Goals.
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