Regulatory submissions of ICSRs in PV operations: Scope and Challenges
Given the international dimension of adverse reactions reporting and the
How automation will help to overcome the current challenges in pharmacovigilance (PV) operations
Pharmacovigilance (PV) is defined as the science and activities relating
Operational productivity and quality monitoring: An integral part of PV operations
Operational productivity and quality management system is an integral aspect
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
Pharmacovigilance discipline merger with IT would witness major electronic transformation
E2B XML was a remarkable turning point in pharmacovigilance for
Pharma/Biotech Industries to modulate their operations to suit the massive pharmacovigilance headway
Product safety has geared up to what we call ‘optimal’
Questions & Answers Blog on recent webinar on ‘Impetus to Literature surveillance in pharmacovigilance on wheels of automation’
These are few of the questions raised by Webinar audience
Automated Safety Reporting Systems: A leap to advancement in Pharmacovigilance
Regulatory deviations that need major corrective actions require huge investment