EXTEDO, a provider of eRegulatory Affairs solutions, has launched MPDmanager to help life sciences firms comply with new European drug safety regulations.
The new solution will support the new XEVMPD submission standard, which goes into effect on 2 July 2012.
The new XEVMPD regulation mandates that life sciences firms use a globally harmonized exchange format to manage drug safety product information.
The application enables companies to manage and submit all regulatory data in the format requested by the XEVMPD and IDMP.
The MPDmanager is part of the EXTEDO Registration Management Suite, and shares the Records Master Data Management layer with other EXTEDOsuite components or third party products, the company said.
EXTEDO CEO Tore Bergsteiner said: "MPDmanager is an intuitive solution that enables life sciences firms to immediately start submitting all of their product information in the new format specified by EMA."