Literature Monitoring

Staying ahead in pharmacovigilance means staying informed. Literature monitoring is a vital component of drug safety that involves the systematic review of scientific publications, clinical studies, and medical journals to detect safety signals, assess emerging risks, and evaluate efficacy trends. This ongoing surveillance ensures that all relevant findings are captured, analyzed, and reported in compliance with global regulatory standards.

For Marketing Authorization Holders (MAHs), regular and thorough review of both global and local literature is not just a requirement—it’s a responsibility. Our team ensures that every piece of relevant data is identified and addressed with precision and speed.

Our Literature Monitoring Services Include:

• Tailored Search Strategy Development
• Global Literature Screening & Review
• Local Literature Monitoring as per Country-Specific Regulations
• Continuous Medical Literature Surveillance
• End-to-End Safety Data Extraction & Reporting
• Monitoring of Non-Traditional Sources (including social media)

Our dedicated literature surveillance experts leverage powerful global databases and region-specific sources to provide complete, compliant, and proactive coverage—helping you maintain product safety and meet regulatory expectations with confidence.