Get the right treatment to the right patient at the right time

<p>Turn siloed, regulated data into AI-ready insight that speeds discovery and improves outcomes.</p>
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Where we operate

R&D and drug discovery

Find better targets, faster. Multi-omics target ID, SAR mining and ADMET-ready data.

Clinical trials

A real-time view into every trial. CDISC data management, query reduction and medical coding.

Regulatory and submissions

Less time on compliance, more on patients. GenAI submission authoring and eCTD structuring, source-traceable.

Pharmacovigilance and drug safety

Solve safety problems before they start. Case intake, MedDRA coding and earlier signal detection.

Commercial operations and market access

Reach the right HCP, the right way. HCP, payer and patient 360, RWE, HEOR and next-best-action.

Supply chain and manufacturing

Demand forecasting, batch/CAPA analytics and cold-chain visibility.

THE WORLD'S TOP COMPANIES TRUST EXL

Trusted by global brands

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"$20M+ annual uplift from HEOR and market-access studies."

"60–80% less manual reconciliation, 100% audit lineage."

"50–70% faster AI-ready data across the value chain."

Gain the benefits of working with EXL

"First value in an 8–12 week POC, 2–5× pilot ROI."

"Proven across pharma, biotech and medtech - 25+ years’ delivery."

"Empowered teams with EXLdata.ai agents and GenAI accelerators."

Teaming with <br><span class="wm-orange-text">top partners</span>

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Frequently asked 
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EXL helps research teams find better targets, faster. EXLdata.ai unifies expert-curated multi-omics, assay, and literature data into one governed knowledge graph for target identification. Teams mine structure-activity relationships and get AI-ready data 50-70% faster, freeing scientists to focus on discovery.

EXL gives sponsors a real-time view into every trial. We map electronic data capture, lab, imaging, and electronic clinical outcome assessment data to Clinical Data Interchange Standards Consortium (CDISC) standards with expert medical coding. The result is fewer queries, 60-80% less manual reconciliation, and a cleaner, faster database lock.

EXL helps teams author submissions 20-40% faster, so they spend less time on compliance and more on patients. Generative AI drafts electronic Common Technical Document (eCTD) dossiers grounded in your standard operating procedures. Every statement is source-traceable and expert-reviewed, giving regulators clear, defensible content.

EXL helps safety teams solve problems before they start. Clinicians adjudicate case intake and apply Medical Dictionary for Regulatory Activities (MedDRA) coding, while AI scans literature and real-world data to surface signals earlier. The result is faster, more consistent case processing and stronger patient protection.

EXL helps commercial teams reach the right healthcare professionals, the right way. We build a trusted 360-degree view of prescribers, payers, and patients to power next-best-action engagement. Our health economics and outcomes research and market access studies deliver more than $20 million in annual revenue uplift.

EXL helps you know what you need, when you need it. We connect demand, batch, quality, and cold-chain data to sharpen forecasting and speed corrective and preventive actions. Built to fit Good Manufacturing Practice requirements, our analytics help reduce shortages, protect product quality, and keep therapies moving to patients.

EXL builds compliance into every model. Domain experts red-team, evaluate, and ground-truth AI outputs, with humans in the loop at critical decision points. Full audit lineage across 100% of regulated data supports GxP, 21 CFR Part 11, and ALCOA+ requirements, so you can scale AI with confidence.

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Let's <span class='o_highlight'>solve together</span>

Combine human ingenuity with advanced AI to discover faster, keep patients on therapy, and grow with confidence.

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