A business leader, a colleague and a physician review a tablet together in a bright hospital corridor

RAiL: Responsible AI in Life Sciences

Report 2026:

Defining an Agentic AI
Trust Benchmark

Executive Summary

Agentic AI is moving into life sciences commercialization faster than the industry has developed a consistent way to evaluate it. To understand what leaders need from these tools and systems, we spent the first half of 2026 listening to the people responsible for putting them to work.

Through the Responsible AI in Life Sciences (RAIL) roundtable series, we spoke with over 80 leaders across North America and Europe in commercial, medical affairs, patient services, IT, and regulatory roles at pharmaceutical, biotech, and medical device companies to gather candid perspectives on responsible AI in commercialization. This insight was expanded with an online survey distributed to the same audiences profile, garnering over 100 qualified respondents.

We found that the debate has already moved past whether to use agentic AI or not. The potential impact of agentic AI to improve both upstream and downstream commercial work is understood. Instead, leaders were wrestling with a harder, more practical question: which agentic AI solutions are trustworthy enough to scale? They could see the potential for business and patient impact. But they also needed to know how to validate vendor claims, maintain oversight, and manage risk as AI agents take on field and patient-facing work.

Today, there is no shared language for distinguishing a robust agentic AI system from a white-labelled chatbot, or an agreed bar for what “responsible AI” means in practice. That makes it difficult for Life Sciences teams to compare vendors’ claims and assess the risks.

This report offers a way to make those judgments. The practical question is not, “Is AI perfect?” but, “Is it safer, better, faster, or more effective than how the work is done today?” Answering it requires clear governance, validation criteria, risk thresholds, and business cases suited to a highly-regulated industry.

The concerns and requirements leaders raised shaped the RAIL Score: a rubric covering the six components of responsible agentic AI against defined criteria. It produces a single, comparable way to assess any agentic AI system or tool — moving the conversation from vendor claims and broad principles to evidence and measurable standards.

Our hope is that leaders use the RAIL Score with their teams to assess any AI solution they use or are considering—so they can see where it stands, what needs to improve, and whether it is ready to scale in Life Sciences.

-Parth Khanna | CEO, ACTO

A life sciences manager reviews a tablet with two clinicians in a bright hospital corridor

Research
Methodology

How the study was conducted

This research combined three methods to gather both depth and breadth of perspective on responsible AI in Life Sciences, focused on commercialization. Perspective was gathered from leaders at pharmaceutical, biotech, and medical device companies from commercial, medical affairs, patient services, and market access, as well as the IT and governance functions behind them.

At a glance:

roundtables
08
cities
08
leaders
80
regions
02
survey respondents
135
  1. Executive
    Roundtables

    80 senior leaders

    hosted at in-person roundtables across 8 cities in North America and Europe with discussions focused on human-centric change, safety, governance & compliance, and AI use cases & impact.

  2. Online
    Survey

    135 respondents

    across the industry from North America and Europe answered 14 multiple-choice questions about Responsible AI in Life Sciences, fielded June–July 2026.

  3. Source
    Synthesis

    Coding of all 8 roundtable transcripts into recurring themes were cross-referenced against the online survey results and existing standards (ISO/IEC 42001, EU AI Act).

Who took part

The roundtables and the survey convened senior leaders spanning large pharma, mid-cap and emerging biotech, and medical device firms.

By Function

Commercial / Commercial Excellence

Roundtables30%
Survey21%

Medical Affairs

Roundtables20%
Survey15%

IT / Data / AI & Governance

Roundtables20%
Survey—

Marketing / Omnichannel / Customer Engagement

Roundtables15%
Survey6%

Market Access & Value

Roundtables8%
Survey—

Legal / Compliance / Regulatory

Roundtables7%
Survey23%

Learning & Development

Roundtables—
Survey23%

Other

Roundtables—
Survey12%

By Industry

Large pharma (>$5B revenue)

Roundtables45%
Survey21%

Mid-cap / emerging biopharma

Roundtables30%
Survey48%

Medical device

Roundtables12%
Survey14%

Advisory / consulting / other

Roundtables13%
Survey17%

By Region

North America

Roundtables6 cities
Survey70%

Europe

Roundtables2 cities
Survey18%

Asia

Roundtables—
Survey12%

By Role

C-suite / Head / VP

Roundtables55%
Survey56%

Director / Senior Director

Roundtables35%
Survey41%

Manager / other

Roundtables10%
Survey3%