RIM

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 entry in RIM system


Back