Literature Monitoring Services

Literature monitoring involves the systematic review of scientific journals, publications, and medical databases to identify safety information relevant to medicinal products or medical devices. This process plays a critical role in pharmacovigilance, enabling the timely detection of adverse events, safety signals, and new medical insights. Key aspects of literature monitoring:

• Global and local monitoring: Tracking publications from international and region-specific sources.
• Adverse event detection: Identifying and reporting safety signals or adverse drug reactions (ADRs).
• Medical information solutions: Extracting relevant clinical data to support product safety and regulatory submissions.
• Regulatory compliance: Ensuring alignment with EMA, FDA, and other global pharmacovigilance requirements.
• Customized reporting: Delivering tailored literature reports based on your product portfolio and markets.

Discover why literature monitoring is essential