Advancing Drug Safety The Role of Literature Surveillance in PV

1. We Offer Quality, Commitment And Customer Satisfaction Advancing Drug Safety: The Role of Literature Surveillance in PV +1 617-657-4781 20-22 Wenlock Road, London N1 7GU, UK www.pubhive.com

2. About Us • We are a cloud-based software-as-a-service (SaaS) company with offices in the United Kingdom (UK), United States, and India. • At PubHive, we are dedicated to revolutionizing the life sciences industry through intelligent workflow automation solutions. Our mission is to empower research and compliance teams with cutting-edge tools that streamline processes, enhance efficiency, and ensure accuracy in every step of their journey. • Our mission is to make healthier scientific literature and information pathways for life science companies of all sizes across all stages of the commercialization lifecycle – from discovery to post-market. • Our management team possesses more than 40 years of combined hands-on expertise in architecting and delivering software solutions to 84% of the world’s top-25 life science companies, dozens of medical device and diagnostics companies, and hundreds of start-up biotechs. +1 617-657-4781 20-22 Wenlock Road, London N1 7GU, UK www.pubhive.com

3. Advancing Drug Safety: The Role of Literature Surveillance in PV • In the rapidly evolving world of healthcare, ensuring the safety of pharmaceutical products is paramount. Effective pharmacovigilance - the science and activities related to detecting, assessing, understanding, and preventing adverse effects - requires more than just monitoring reports from clinical settings.  • Literature surveillance has emerged as a vital component in the pharmacovigilance toolkit, providing a proactive approach to identifying and mitigating risks associated with drug therapies. Learn More +1 617-657-4781 20-22 Wenlock Road, London N1 7GU, UK www.pubhive.com

4. What is Literature Surveillance in Pharmacovigilance? • Literature surveillance involves continuously monitoring scientific and medical literature to detect information on adverse drug reactions (ADRs) and other safety signals. • This process entails reviewing published research, case reports, clinical trials, and other scientific documents that discuss a drug's safety and efficacy. • Regulatory authorities, such as the FDA and EMA, mandate literature monitoring in pharmacovigilance as a requirement, underscoring its critical role in safeguarding public health. +1 617-657-4781 20-22 Wenlock Road, London N1 7GU, UK www.pubhive.com

5. Why Literature Surveillance Matters • Literature surveillance provides individual case reports from healthcare providers, scientific literature encompasses a broader range of studies, including long-term clinical trials, population studies, and case series, each providing comprehensive data on drug interactions, side effects, and potential off-label uses. Through proactive monitoring of scientific publications, organizations can: • Identify Emerging Safety Signals Early: Literature surveillance enables organizations to detect potential ADRs and other safety signals that might be missed in clinical settings. • Meet Regulatory Compliance: By staying on top of regulatory requirements, companies demonstrate their commitment to drug safety, building trust with regulators and the public. • Optimize Risk Management Strategies: The data from literature surveillance can guide risk management strategies, such as updating drug labels, issuing safety warnings, or conducting further research. +1 617-657-4781 20-22 Wenlock Road, London N1 7GU, UK www.pubhive.com

6. How Technology is Transforming Literature Surveillance • Advancements in technology have revolutionized how pharmacovigilance teams conduct literature surveillance. Automated systems like PubHive Navigator enable teams to efficiently monitor thousands of publications, categorize them based on relevance, and track emerging patterns in ADRs. These platforms leverage AI-driven algorithms to flag relevant studies, saving time and enhancing accuracy in the review process. With such tools, pharmacovigilance teams are empowered to: • Improve Efficiency: Automated literature monitoring drastically reduces the time spent manually reviewing documents, allowing teams to focus on high-impact tasks. • Ensure Consistency: AI-driven tools apply consistent criteria in assessing literature, ensuring uniformity in signal detection and risk assessment. • Enhance Collaboration: Cloud-based solutions, like those offered by PubHive, foster collaboration by enabling multiple team members to access and update findings in real-time. +1 617-657-4781 20-22 Wenlock Road, London N1 7GU, UK www.pubhive.com

7. Conclusion • The role of literature surveillance in advancing drug safety is undeniable. As a cornerstone of effective pharmacovigilance, pharmaceutical companies can stay ahead of potential risks, ensuring that patients receive the safest and most effective therapies possible. • With tools like PubHive Navigator, organizations can transform their approach to literature surveillance -moving from reactive to proactive pharmacovigilance. By continuously monitoring the wealth of information available in scientific literature, the industry can achieve higher standards of drug safety and work towards a future where adverse drug reactions are minimized and patient trust is strengthened. • Explore how PubHive’s technology can revolutionize your approach to literature surveillance and pharmacovigilance. +1 617-657-4781 20-22 Wenlock Road, London N1 7GU, UK www.pubhive.com

8. Contact Us Contact No +1 617-657-4781 Website Link www.pubhive.com Address 20-22 Wenlock Road, London N1 7GU, UK