Branded softwares in Pharmacovigilance: Are we being unduly ‘overgenerous’ in name of Regulatory compliance!
This blog presents Industry expert’s views and expresses their opinions
Gearing up for a smooth transition to ISO-IDMP standards: Planning step-wise
In pharmacovigilance and in this industry largely, striking a regulatory
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
Surpass limitations of Literature monitoring in Drug safety with flexible and versatile approach
With the advent of technology, we are cocksure to upgrade
Questions & Answers of webinar (Feb 2015) on Signal detection methodology: Current and Novel approaches
This Questions & Answers Blog are from Signal Detection Webinar
Medicinal product ‘inquiry’ centers: An infallible mechanism to combat efficacy, safety, quality and other product challenges
If a Marketing Authorization Holder (MAH) nurtures a molecule and
Things You should know about Pharmacovigilance ‘Signal’!
Signal detection and validation by Marketing Authorization Holders is an
Automated Safety Reporting Systems: A leap to advancement in Pharmacovigilance
Regulatory deviations that need major corrective actions require huge investment
Paper-based systems in an era of e-Pharmacovigilance is but a tortoise pace
Well-defined pharmacovigilance systems and transparent data analysis need no deeper