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  • Can AI Replace Medical Information Specialists? Opportunities, Risks, and Reality

    October 29, 2026

    AI in Medical Information is transforming how pharmaceutical companies respond to healthcare professionals, patients, and caregivers. From intelligent scientific search to AI-generated responses, new technologies promise greater efficiency and lower operational costs. But this raises an important question: Can AI replace medical information specialists, or will it simply change how they work? The answer is…

    Read more: Can AI Replace Medical Information Specialists? Opportunities, Risks, and Reality
    Can AI Replace Medical Information Specialists? Opportunities, Risks, and Reality
  • AI-Designed Antibiotics: What Gonorrhoea and MRSA Breakthroughs Mean for Pharma R&D

    August 25, 2025

    AI-Designed Antibiotics are no longer science fiction — they are here. In a landmark MIT study published in Cell, generative AI created two novel compounds capable of killing drug-resistant gonorrhoea and MRSA in laboratory and animal tests. This achievement not only demonstrates the power of AI in antimicrobial research but also signals a potential turning…

    Read more: AI-Designed Antibiotics: What Gonorrhoea and MRSA Breakthroughs Mean for Pharma R&D
  • The EU AI Act and Pharma Compliance: What Life Sciences Companies Need to Know

    July 9, 2025

    The EU AI Act is reshaping how pharmaceutical and life sciences companies develop and deploy AI — from clinical trials to diagnostics. As the world’s first comprehensive AI regulation, it introduces strict rules around risk classification, human oversight, and audit trails. If your company is building AI-powered tools or seeking approval in the EU and…

    Read more: The EU AI Act and Pharma Compliance: What Life Sciences Companies Need to Know
    The EU AI Act and Pharma Compliance: What Life Sciences Companies Need to Know
  • FDA AI Food Safety: How ELSA is Changing Import Oversight

    July 7, 2025

    Summary:FDA ELSA AI food safety efforts mark a turning point in how the agency screens food imports, using machine learning to flag high-risk shipments. In June 2025, the FDA announced the agency-wide launch of a powerful new AI tool named ELSA (Enhanced Learning and Surveillance Algorithm). Designed to improve how the FDA screens imported foods,…

    Read more: FDA AI Food Safety: How ELSA is Changing Import Oversight
    FDA AI Food Safety: How ELSA is Changing Import Oversight
  • FDA’s 2025 Draft Guidance on AI in Drug Development: What It Means for Biopharma

    July 3, 2025

    AI in drug development is rapidly transforming how therapies are discovered, tested, and submitted for approval—but until now, regulatory guidance has struggled to keep up. That changed in January 2025, when the U.S. Food and Drug Administration (FDA) published its first-ever draft guidance focused on the use of AI to support regulatory decision-making in the…

    Read more: FDA’s 2025 Draft Guidance on AI in Drug Development: What It Means for Biopharma
    FDA’s 2025 Draft Guidance on AI in Drug Development: What It Means for Biopharma

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