Overview
Trially.ai, an AI-powered clinical trial recruitment platform built by veterans from Epic, Cerner, and Zapier, partnered with Disrupt to build a content presence as sophisticated as its technology. The company needed a medical copywriting partner who could translate deeply technical, heavily regulated subject matter spanning AI, EHR architecture, and compliance frameworks such as HIPAA and FDA 21 CFR Part 11 into clear, credible content that could pass formal review. Disrupt delivered a library of compliance-reviewed blogs, white papers, and newsletter content that positions Trially as a credible leader in AI-powered recruitment.
The Challenge
Clinical trial recruitment is one of the most technically complex and heavily regulated spaces in healthcare, and Trially's content had to reflect that reality. With a sophisticated audience of sponsors, CROs, research coordinators, and healthcare executives, generic health content would not suffice. The company needed:
A medical copywriting partner fluent in AI, large language models, EHR architecture, and clinical research methodology
Content that translated deeply technical subject matter into clear, credible, and compelling writing
Strict adherence to regulatory and compliance standards, including HIPAA, SOC 2, FDA 21 CFR Part 11, and ISO 27001
Formal compliance review was built into the process for every piece before publication
The Disrupt Solution
Our work with Trially spanned three content formats, each serving a distinct role in their broader content and thought leadership strategy.
Blogging
The foundation of the engagement was a series of SEO blog posts covering the full breadth of Trially's platform and the clinical trial recruitment landscape in which it operates. Topics ranged from AI versus manual patient prescreening and the implications of landmark clinical research published in the Journal of the American Medical Association, to EHR data architecture, physician engagement barriers, data security infrastructure, and the future of protocol feasibility assessment. Each post required original research, precise technical language, and careful adherence to Trially's regulatory disclaimers and compliance standards, all while remaining accessible and engaging for readers across multiple professional backgrounds.
Whitepaper(s)
Alongside the blog program, we developed a series of strategic white papers examining AI's role in transforming clinical trial recruitment, designed as gated assets for key stakeholders, including sponsors, CROs, and research institutions. The white paper required the depth, authority, and rigor that the format demands, combining industry data, regulatory context, and forward-looking analysis into a single high-impact resource built to reinforce Trially's position as a credible leader in AI-powered recruitment solutions.
Email Newsletter
We also supported Trially's LinkedIn newsletter, producing content tailored to their professional audience and aligned with the thought-leadership positioning established across the broader content program.
Trially
Building Authoritative Content for AI-Powered Clinical Research
The Results
Across blog posts, a strategic white paper, and LinkedIn newsletter content, MedCopy helped Trially build a content presence that matches the sophistication of the platform it represents. A technically complex and highly regulated product now has a library of compliance-reviewed content that speaks with authority to the clinical research professionals Trially is built to serve. Each piece helped advance the same core narrative: AI-powered recruitment is not a future concept but a present, proven solution, and that Trially is the team best positioned to deliver it.
For potential clients evaluating Trially's capabilities, that content library functions as both education and evidence.
Project Details at a Glance:
~10 SEO blog posts produced across AI technology, regulatory compliance, clinical methodology, EHR architecture, and data security
2 strategic white papers developed as a gated stakeholder asset
LinkedIn newsletter content produced for a professional audience distribution
All content is compliant with HIPAA, SOC 2, FDA 21 CFR Part 11, and ISO 27001 standards
Full multi-stage compliance review completed across all deliverables