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    Generative AI-Powered Medical Affairs Assistant

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    Revolutionize how Medical Affairs teams interact with scientific and regulatory data. This generative AI-powered professional service delivers intelligent, evidence-backed insights that streamline literature reviews, enhance decision-making, and ensure regulatory compliance.

    Overview

    Overview

    Built on advanced generative AI and hosted on scalable AWS infrastructure, this solution empowers Medical Affairs teams to efficiently navigate complex scientific literature and regulatory documentation. By automating data synthesis, summarization, and citation generation, it reduces manual effort and accelerates strategic planning. The assistant supports natural language queries, adapts to evolving healthcare needs, and ensures compliance with scientific and regulatory standards - making it a high-impact tool for life sciences organizations.

    Key Features

    • Natural Language Query Engine

    Ask complex medical and regulatory questions in plain language and receive clear, evidence-backed responses.

    • Cross-Document Insight Synthesis

    Automatically combine information from multiple sources to build a comprehensive understanding of scientific topics.

    • Automated Summarization

    Generate concise summaries from lengthy literature and regulatory documents, tailored to specific queries.

    • Regulatory Compliance Alignment

    Ensure outputs meet scientific and regulatory standards using fine-tuned, domain-specific AI models.

    • Citations Generator

    Automatically create properly formatted references with traceable source metadata for documentation and reporting.

    • Customizable Dashboards

    Visualize insights, track queries, and manage workflows through role-specific dashboards.

    Use Cases

    This solution supports a wide range of roles across healthcare and life sciences:

    • Medical Affairs Teams: Accelerate literature reviews, regulatory Q&A, and strategic planning

    • Pharmaceutical Companies: Support drug safety analysis, efficacy reviews, and post-market surveillance

    • Regulatory Agencies: Validate compliance and streamline documentation processes

    • Clinical Research Organizations: Synthesize evidence across studies and generate insights for trial design and reporting

    • Healthcare Providers: Access decision support for treatment protocols and clinical guidelines.

    Benefits

    • Save Time & Resources

    Automate manual research tasks to reduce effort and improve productivity

    • Improve Decision-Making

    Access synthesized, evidence-backed insights for faster and more informed decisions

    • Ensure Regulatory Compliance

    Built-in alignment with scientific and regulatory standards reduces risk and review cycles

    • Scale Across Teams and Geographies

    Modular architecture and multilingual support enable global deployment

    • Focus on Strategic Initiatives

    Free up teams to concentrate on high-value activities like stakeholder engagement and innovation

    Key AWS Components

    Amazon Bedrock / SageMaker, Amazon RDS, Amazon CloudWatch, AWS IAM, Amazon EventBridge, Amazon SNS, Amazon S3, AWS Lambda, Amazon OpenSearch, Amazon Secrets Manager.

    Highlights

    • Generative AI Agents: Controller, Retriever, Synthesizer, and Citations agents working in harmony
    • Natural Language Intelligence: Ask, retrieve, and synthesize with ease
    • Built-In Compliance: Fine-tuned models ensure regulatory alignment

    Details

    Delivery method

    Deployed on AWS

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    Pricing

    Custom pricing options

    Pricing is based on your specific requirements and eligibility. To get a custom quote for your needs, request a private offer.

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