One of our Qdossier members (Marloes van der Geer) will be attending the DIA Europe meeting, taking place in Brussels this year. In case you are interested to meet someone […]

At DIA’s Regulatory Submissions, Information, and Document Management (RSIDM 2022) Forum, we will hear from industry and regulatory stakeholders working across the scope of regulatory information to examine current and […]

Join us in an interactive two-day course that will provide you with a clear and comprehensive understanding of the regulatory and technical requirements for CMC management of your full and generic […]