Product Inquiry Trail and Response system (PrITR)
Management of medical inquiries, product complaints and adverse events due
PvD’code: A Smart EV triage solution
New Eudravigilance system was launched on November 22nd, 2017, and a prominent
Automated literature surveillance: A much needed enhancement for Marketing authorization holders and Service providers in pharmacovigilance (PV)
The medical literature monitoring (MLM) is a significant source of
Artificial intelligence and Machine learning in Pharmacovigilance (PV) operations
Much of the effort in PV is focused on identifying,
Continuous refinement of Pharmacovigilance regulations in Arab countries
Pharmacovigilance (PV) significance and cognizance is constantly growing amongst pharma
Veterinary Pharmacovigilance – Few guidance extracts
Veterinary medicinal products (VMPs) also require safety monitoring to addresses
Pooling meaningful data from vast Pharmacovigilance database for Regulatory periodic reports
There exist regional and universal guidelines emphasizing the type and
Mechanism to extract adverse experience reports output for US FDA
Periodic safety reports are prepared as a part of periodic
Solution to Periodic safety submissions (PADER/PAER reports) through eCTD submission software
The Regulatory industry is witnessing huge transformations. Some new regulations
Pharmacovigilance discipline merger with IT would witness major electronic transformation
E2B XML was a remarkable turning point in pharmacovigilance for