Do not hesitate to contact us, if you seek for help in:

  • Delivering regulatory submissions reliably and on time

  • Regulatory Information Management (RIM): management of the regulatory activities during the complete life cycle of the medicinal product

  • Consultancy in the vendor selection for new RIM system

  • Support in choosing the right eCTD tool for your company

  • Implementation, migration, test and validation of Regulatory systems

  • Consultancy in the implementation of EDMS (Documentum / FirstDoc, Veeva Vault, SharePoint)

  • Consultancy in IDMP

  • Data mapping

  • Data entry in RIM system