Regulatory Submissions, Information, and Document Management Forum

How regulatory information is managed has a profound impact on operational efficiency across the whole organization, on data quality, and ultimately on the company’s ability to meet the needs of patients. As global regulatory requirements, technology, data sources, and data standards evolve, the importance of sound regulatory information management becomes even greater.

DIA’s Regulatory Submissions, Information, and Document Management (RSIDM) Forum brings together industry and regulatory stakeholders working across the scope of regulatory information to examine current data standards and requirements and effective regulatory information management approaches to align related systems. The Forum presents four tracks: Regulatory Information Management (RIM) Business, RIM Technology, Electronic Document Management, and Electronic Regulatory Submissions.

A  delegation of Iperion will be present during DIA.

Frits Stulp – Managing director

Remco Munnik – Associate director

Lise Stevens – Associate director

Please reach out to us for a catch up during lunch, to grap a cup of coffee or a meeting. We are happy to meet you!

More information and subscribe


10 - 12 Feb 2020





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