IDMP (in Pipline)

IDMP (in pipeline)

We bring in the expertise in solutioning and implementing the Global Regulations on Safety Reporting like the upcoming IDMP. Our team has proven track record in similar solutions implementations like EMA EDQM, MFDS, NMPA, FDA Combo Vaccine etc.
  • Organizational Master Database creation and maintenance with SPOR Data 
  • Ensuring timely and accurate updates of the SPOR data into the Master Database 
  • Submitting org-level SPOR data to EMA SMS, PMS, OMS, and RMS systems to get the Product related IDs from EMA 
  • Comparing the data received from EMA with the available data in the org master database 
  • Using the Product related IDs (MP ID, PC ID, Php ID, Substance ID) received from EMA for case submissions to meet compliance