AI-assisted SLR for a breakthrough therapeutic

FIECON is supporting a breakthrough therapy in the accelerated approval regulatory process by assembling a global evidence package to expedite EMA submission and approval alongside the FDA.
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Technical Ability

We are technically astute, with experts who bring deep healthcare strategy and clinical knowledge to every project.

AI-assisted SLR

We conduct SLRs to HTA using AI technology, addressing:
  • Adherence to HTA by completing all systematic review steps to meet evidentiary requirements.
  • A unified SLR protocol, incorporating multi-database searches, quality-controlled screening, and meta-analyses of RCTs.
  • Standardized, replicable templates leveraging dynamic HTA formats and workflows to satisfy HTA needs.
  • Harmonized HTA, aligning with JCA requirements for 2025.

Infrastructure for replicable SLRs for HTA and PICOs

  • We define clinical lexicons and ontologies by disease state.
  • We create templates for HTA archetypes and scientific platforms, and adapt past projects for regulatory use.
  • We execute AI-assisted SLRs in real time, satisfying 10+ PICOs across multiple markets.

Practical Agility

Accelerating business objectives in tight timelines:

We shorten timelines by eliminating duplicative efforts across departments and embedding scientific best practices.

We leverage the newest AI technology to meet key business goals efficiently.

Relevant resources

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Get a completely free, no-obligation opportunity to discuss your needs and see how we can boost your business.
  • Brainstorm solutions to key challenges with experienced team
  • Validate your strategy and value evidence
  • Learn more about FIECON’s products and key areas of expertise and discuss opportunities for collaboration

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