Literature Surveillance

Staying Ahead with Comprehensive Literature Monitoring

In the fast evolving world of clinical research, staying informed about the latest scientific and medical literature is crucial for making evidence based decisions and ensuring regulatory compliance. At Safevigilance, our Literature Surveillance Services provide thorough and systematic monitoring of relevant literature to support your clinical trials, enhance safety, and drive innovation. Our expert team ensures you remain updated with the latest research developments, emerging trends, and potential risks.

1. Systematic Literature Review

Conduct comprehensive reviews to gather relevant and uptodate information:
  • Targeted Searches: Perform targeted literature searches based on specific therapeutic areas, clinical conditions, or research questions.
  • Database Access: Utilize a wide range of scientific databases and resources, including PubMed, Embase, and Cochrane Library.
  • Review and Analysis: Analyze and summarize findings from relevant studies, systematic reviews, and metaanalyses.

2. Risk Identification and Signal Detection

Identify potential safety signals and emerging risks from the literature:
  • Safety Signal Detection: Monitor and detect new safety signals or adverse effects related to your drug or intervention.
  • Trend Analysis: Analyze literature trends to identify any changes in safety profiles or efficacy concerns.
  • Risk Assessment: Assess potential risks identified through literature surveillance and provide actionable insights.

3. Regulatory Compliance Support

Ensure compliance with regulatory requirements for literature monitoring:
  • Regulatory Updates: Track and summarize regulatory guidance and requirements related to literature surveillance and safety monitoring.
  • Submission Support: Assist with literature based components of regulatory submissions, such as periodic safety reports and updates.
  • Documentation: Maintain comprehensive documentation of literature searches, findings, and analyses for regulatory review.

4. Competitive Intelligence

Gain insights into the competitive landscape and industry advancements:
  • Competitor Analysis: Monitor and analyze literature related to competitors’ products, clinical trials, and research activities.
  • Market Trends: Identify and assess market trends and innovations that may impact your clinical development strategy.
  • Strategic Insights: Provide strategic insights based on literature findings to inform your product development and positioning.

5. Customized Reporting and Alerts

Receive tailored reports and alerts based on your specific needs:
  • Customized Reports: Generate customized literature reports highlighting key findings, trends, and safety signals relevant to your trial or therapeutic area.
  • Alerts and Notifications: Set up alerts for new publications, updates, or significant findings in areas of interest.
  • Periodic Updates: Provide regular updates and summaries to keep you informed of the latest literature developments.

6. Expert Consultation and Analysis

Access expert analysis and consultation to interpret literature findings:
  • Expert Analysis: Receive expert analysis of literature findings to support decisionmaking and strategy development.
  • Consultation Services: Consult with our team of experts for indepth discussions and interpretations of literature data.
  • Strategic Recommendations: Get actionable recommendations based on literature surveillance to enhance trial safety and efficacy.