{"id":5933,"date":"2026-04-01T08:42:18","date_gmt":"2026-04-01T08:42:18","guid":{"rendered":"https:\/\/globalnewstoday.uk\/index.php\/2026\/04\/01\/ai-led-selloff-in-contract-research-firms-may-be-misjudging-disruption-risk-wtaq\/"},"modified":"2026-04-01T08:42:18","modified_gmt":"2026-04-01T08:42:18","slug":"ai-led-selloff-in-contract-research-firms-may-be-misjudging-disruption-risk-wtaq","status":"publish","type":"post","link":"https:\/\/globalnewstoday.uk\/index.php\/2026\/04\/01\/ai-led-selloff-in-contract-research-firms-may-be-misjudging-disruption-risk-wtaq\/","title":{"rendered":"AI-led selloff in contract research firms may be misjudging disruption risk &#8211; WTAQ"},"content":{"rendered":"<p>By Kamal Choudhury and Siddhi Mahatole<br \/>March 31 (Reuters) \u2013 Shares of contract research organizations have tumbled on fears that advances in artificial intelligence could allow drugmakers to take clinical trial work in-house, but industry experts say the selloff overestimates how far the technology can replace the sector\u2019s core capabilities.<br \/>IQVIA, Medpace and Charles River Laboratories have fallen \u200bsharply since Anthropic\u2019s launch of advanced AI agents in February fuelled expectations that drugmakers could rely less on \u200cCROs.<br \/>A recent wave of partnerships between pharmaceutical companies and AI firms has further added to those worries.<br \/>\u201cCould AI eat CROs? Yeah, I think that could be a possibility,\u201d said Thomas Laur, CEO at data analysis firm DNAnexus.<br \/>But the nature of services that CROs provide, from patient recruitment to global trial execution, will be difficult to automate or replace, several analysts, industry experts and policy makers told Reuters.<br \/>CROs maintain global networks of trial sites and hold \u200cproprietary data \u200bthat pharma companies, especially smaller biotechs, cannot easily replicate, Jailendra Singh, analyst at \u2060Truist Securities, said.<br \/>That view is echoed across \u2060Wall Street. Analysts at TD Cowen estimate that even a fully AI-enabled clinical trial setup would deliver only 10%\u201315% cost savings for drugmakers.<br \/>At the core of the argument is the pharmaceutical industry\u2019s reliance on execution at scale.<br \/>Finding even a small pool of eligible patients for an early trial, across diverse demographics and geographies, requires enormous data and site networks that \u200bCROs have built over decades. \u201cPharma companies do not have that same level of data and expertise,\u201d Singh added.<br \/>HUMAN ELEMENT<br \/>Executives of CROs say AI may streamline parts of the process, but cannot replace the human and operational backbone of trials.<br \/>\u201cAI itself can\u2019t reach \u2060out to the doctor, enroll the patient, make sure they show up \u2060to the appointment on time, record all the data,\u201d said Brigham Hyde, CEO of Atropos Health.<br \/>Although \u200bAI could automate high-volume tasks such as patient pre-screening, critical decisions still require human oversight, said Ami Bhatt, chairperson of U.S. FDA\u2019s \u200bDigital Health Advisory Committee.<br \/>Site execution, informed consent and safety monitoring remain firmly in human hands, she said, \u200cwith accountability ultimately resting on people.<br \/>Others point to more fundamental constraints with the technology. AI cannot replace laboratory testing required for drug safety, and its use in direct patient care remains limited by regulatory scrutiny and liability risks, said William Pierce, a former deputy assistant secretary of public affairs at the Department of Health and Human Services.<br \/>OPPORTUNITY AHEAD<br \/>Rather than replacing CROs, analysts say AI could enhance \u2060their value by speeding up trials and improving efficiency.<br \/>TD Cowen\u2019s analysts estimate a fully AI-enabled late-stage trial could be completed in 47 months versus a baseline of 58 months, an 11-month reduction.<br \/>That kind of timeline compression could become a powerful competitive advantage for \u2060CROs that invest heavily in AI.<br \/>For instance, reaching \u200cthe market nearly a year earlier for a drug with estimated peak annual revenues of $1.5 \u2060billion could drive roughly $44 million in additional revenue, TD Cowen added.<br \/>\u201cWe expect new types of \u200bcontracting to \u200cemerge, including gain-share arrangements on AI efficiencies,\u201d the brokerage said.<br \/>But the recent stock slide suggests \u200blingering investor unease.<br \/>Jim \u2060Lee, head of Inflammation and Autoimmunity at drugmaker Incyte, said investors are likely worried about the services that CROs may have to scale back, which could affect their revenue.<br \/>For now, analysts maintain there is no evidence of pharma companies cutting spending with CROs because of AI and termed the sell-off as \u201cpanic more than (a) real threat\u201d.<br \/>For Singh, the bottom line is straightforward: \u201cwe do not see AI as a headwind for the industry; if anything, it is more of a tailwind.\u201d<br \/>(Reporting by Kamal Choudhury and Siddhi Mahatole in Bengaluru; Writing by \u200bMrinalika Roy; Editing by Shinjini Ganguli)<br \/>You must be <a href=\"https:\/\/wtaq.com\/login?returnUrl=https:\/\/wtaq.com\/2026\/03\/31\/ai-led-selloff-in-contract-research-firms-may-be-misjudging-disruption-risk\/\">logged in<\/a> to post a comment.<br \/>This site is protected by reCAPTCHA and the Google <a href='https:\/\/policies.google.com\/privacy'>Privacy Policy<\/a> and <a href='https:\/\/policies.google.com\/terms'>Terms of Service<\/a> apply.<\/p>\n<p><a href=\"https:\/\/news.google.com\/rss\/articles\/CBMipwFBVV95cUxNLTgwX1RwNl80X0FhcXhuWjU0Z3ZlZG5wMC1ValZTWW52cldXOWI3R0g3WGJ1Qkh1NzhJb2tvVWQzeXdGSElyZmthcDNGenRVR1IzeUhLNkxQc2phdk5HdEhVNl84YkViTGlLSHo2ZW1zemlQQVNveXh4ZGNGSWVQQWtlZDdiZGd4anB6LVlkdk9hbFlCdWF0SGkzTzZScXBZZXJMMlJRZw?oc=5\">source<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>By Kamal Choudhury and Siddhi MahatoleMarch 31 (Reuters) \u2013 Shares of contract research organizations have tumbled on fears that advances in artificial intelligence could allow drugmakers to take clinical trial work in-house, but industry experts say the selloff overestimates how far the technology can replace the sector\u2019s core capabilities.IQVIA, Medpace and Charles River Laboratories have [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":5934,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[9],"tags":[],"class_list":{"0":"post-5933","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-science"},"_links":{"self":[{"href":"https:\/\/globalnewstoday.uk\/index.php\/wp-json\/wp\/v2\/posts\/5933","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/globalnewstoday.uk\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/globalnewstoday.uk\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/globalnewstoday.uk\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/globalnewstoday.uk\/index.php\/wp-json\/wp\/v2\/comments?post=5933"}],"version-history":[{"count":0,"href":"https:\/\/globalnewstoday.uk\/index.php\/wp-json\/wp\/v2\/posts\/5933\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/globalnewstoday.uk\/index.php\/wp-json\/wp\/v2\/media\/5934"}],"wp:attachment":[{"href":"https:\/\/globalnewstoday.uk\/index.php\/wp-json\/wp\/v2\/media?parent=5933"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/globalnewstoday.uk\/index.php\/wp-json\/wp\/v2\/categories?post=5933"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/globalnewstoday.uk\/index.php\/wp-json\/wp\/v2\/tags?post=5933"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}