INDUSTRIES

Healthcare

Faster trials. Safer submissions.
Revenue you're not leaving uncaptured.

The Challenge

Healthcare and pharma lose billions annually to manual compliance, missed coding revenue and clinical trial inefficiencies.

Pharmacovigilance Burden
Millions of case reports processed manually each year against strict 15-day deadlines - large teams required, compliance risk is material.
Submission Inconsistency
Medical writers spend months on CTD modules - any inconsistency triggers an FDA or EMA deficiency letter and months of costly delay.
Trial Enrolment Gaps
80% of trials miss enrolment targets. Manual site selection and patient screening is labour-intensive and protocol deviations are caught late in data cleaning.
Revenue Leakage
Coding accuracy at 60-80% for complex cases leaves significant revenue uncaptured - NHS backlogs and payer denials compound the exposure.

The Solutions

USE CASE 01

LLM Pharmacovigilance Agent

60-80% faster case processing. Improved compliance. Better safety signal detection at scale.

Pain Point

Pharmacovigilance teams manually review adverse event reports from multiple global sources - narratives, emails, literature. Case processing takes days. Volume is growing. Regulatory submission windows are fixed.

Our Solution

An LLM-powered PV agent reads incoming adverse event narratives, extracts structured case data, maps to MedDRA codes and generates CIOMS/E2B(R3)-ready draft reports - with human reviewer approval as the final set up.

Impact

60% to 80% reduction in case processing time
Improved compliance rate
Faster safety signal detection across large case volumes.
USE CASE 02

Regulatory Submission Agent

50% to 70% faster preparation. Lower per-submission cost. Fewer deficiency letters.

Pain Point

Regulatory submissions - CTDs, INDs, NDAs, MAAs - require months of manual document preparation, inconsistent formatting across contributors, and high rates of deficiency letters from agencies.

Our Solution

An agentic system orchestrates the preparation of regulatory documents by extracting data from CSRs and SAPs, cross-referencing prior approved submissions, applying eCTD formatting and checking compliance against agency guidance - with LLM-assisted narrative drafting.

Impact

50% to 70% reduction in preparation time
Faster time to market
Lower per-submission cost
Reduced deficiency letter rate
USE CASE 03

Clinical Trial Operations Agent

30% to 40% reduction in enrolment timelines. 15% to 25% trial cost reduction. Fewer protocol deviations.

Pain Point

Clinical trial operations teams manage complex, multi-site enrolment manually - identifying sites, screening patients against eligibility criteria, tracking protocol deviations and managing data queries through fragmented systems.

Our Solution

An AI operations agent automates patient screening against eligibility criteria, generates personalised outreach for recruitment, monitors enrolment velocity against targets and flags protocol deviations - across all trial sites simultaneously.

Impact

30% to 40% reduction in enrolment timelines
15% to 25% trial cost reduction
Lower protocol deviation rates and fewer costly amendments
USE CASE 04

Medical Coding & Revenue Cycle Management

92% to 96% coding accuracy. 3% to 8% revenue uplift. 40% to 60% reduction in coding backlog.

Pain Point

Medical coding of clinical notes to ICD-10/CPT is done manually by certified coders - creating backlogs, coding inconsistencies, revenue cycle delays and significant claim denial rates.

Our Solution

An LLM coding agent reads clinical documentation, assigns ICD-10 and CPT codes with confidence scores, flags ambiguous cases for human review and integrates directly with RCM billing systems - closing the loop from encounter to reimbursement.

Impact

Coding accuracy to 92% to 96% accuracy
3% to 7% revenue uplift
30% to 50% reduction in claim denial rates
40% to 60% reduction in coding backlog

Let's explore what's possible together.

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