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Life sciences

Without clarity, there’s no compliance

Infodesk helps pharmaceutical, biotech, biomedical, medical device and consumer health organizations reduce risk, respond faster, and stay aligned. We turn regulatory complexity into structured, auditable action that drives compliance and confidence.

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The problems slowing you down

The volume and pace of change are accelerating. Infodesk helps regulatory teams reduce compliance risk, coordinate faster, and respond decisively to regulatory developments.

  • Rising complexity in regulatory surveillance

    Agencies like the FDA and EMA issue more updates than ever. Manual tracking makes it easy to miss critical changes that affect development, approval, or compliance.

  • Information overload and fragmentation

    Teams juggle alerts from emails, feeds, and third-party sites without filtering, context, or coordination. Important updates get buried in the noise.

  • Delayed and inconsistent communication

    Even when changes are identified, they’re not always shared quickly or with the right stakeholders, slowing response and creating compliance gaps.

  • Strategic blind spots

    Without centralized visibility, organizations risk missing emerging guidance or market trends, especially in global or fast-moving therapeutic areas

Built for how you work

Stay audit-ready while moving fast

Pharma teams use Infodesk to cut manual effort, monitor change, and coordinate across global functions, with traceable records ready for audit or submission.

  • Cut monitoring time with curated, validated updates
  • Track policy changes and trends by product or region
  • Align teams with shared updates and structured workflows
  • Build searchable records for audit, submission, or review
Pharmaceutical

Stay audit-ready while moving fast

Pharma teams use Infodesk to cut manual effort, monitor change, and coordinate across global functions, with traceable records ready for audit or submission.

  • Cut monitoring time with curated, validated updates
  • Track policy changes and trends by product or region
  • Align teams with shared updates and structured workflows
  • Build searchable records for audit, submission, or review
MedTech

Manage change without added complexity

Regulatory professionals use Infodesk to track MDR, IVDR, and global updates while keeping QA, RA, and legal aligned, without added admin.

  • Stay on top of MDR and IVDR developments
  • Create structured cases for faster impact assessments
  • Track submissions, commentary, and procedural updates
  • Share updates with QA, RA, and legal from one platform
Consumer health

Link regulatory change to business impact.

Connect teams across regions and focus areas Infodesk helps regional teams stay aligned, reduce duplication, and act confidently on relevant changes across jurisdictions, product lines, and species.

  • Prioritize changes based on risk, relevance, and regulatory impact
  • Ensure consistent communication with automated alerts
  • Reduce duplication of effort across regions or markets
  • Build confidence with traceable, structured decision records

Why life sciences teams choose us

Streamlined global monitoring

Aggregate updates from health authorities, premium providers, and internal sources into one central view

Faster, more accurate responses

AI-powered filtering and summarization reduce monitoring time by at least 50% and surface only the most critical updates

Seamless communication

Automated newsletters, alerts, and dashboards align regulatory stakeholders quickly and consistently

Audit-ready documentation

Maintain searchable archives and content tagging that support compliance, visibility, and long-term oversight

More ways to work with Infodesk

  • Regulatory Workflow Solution

    Turn updates into action with structured case management, SME tracking, audit-ready records, and real-time visibility – purpose-built for regulatory, quality, and safety teams.

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  • Market intelligence

    Infodesk unifies global market and competitive intelligence, combining AI and analyst validation to deliver timely, verified insights for faster decisions

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  • Regulatory intelligence

    Filter scientific updates by topic, region, or therapeutic area and deliver credible research to stakeholders at speed, with full source transparency

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Intelligence activation for insurance customer stories

Discover more about the Infodesk platform

From intelligence to impact. The Infodesk platform drives informed action for enterprises

  • Monitor

    You can’t confidently manage what you don’t monitor. Infodesk’s surveillance and monitoring capabilities keep you informed and in control

  • Curate

    With AI-powered curation features, Infodesk helps organizations turn complex, high-volume information into decisive, auditable action.

  • Action

    Where intelligence means impact. Infodesk helps convert intelligence into outcomes

Trusted scientific and regulatory content

From policy shifts to safety events, Infodesk delivers validated, compliance-focused intelligence from the sources your teams already rely on.

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Managed professional services

Alongside Infodesk’s monitoring features, our team of analysts, editors, and information specialists combine human expertise with advanced technology to deliver trusted, relevant intelligence. All without added effort on your part. Their oversight ensures intelligence is validated, curated, and always aligned with your priorities.

With backgrounds in analysis, research, journalism, communications, and publishing, our experts act as an extension of your team. They provide timely intelligence that’s ready to use, helping your organization respond faster, reduce manual work, and focus on high-value strategic decisions.

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Human first, always

We use AI to elevate human judgment, not to replace it. In high-pressure environments, explainability matters as much as efficiency.