Guru centralizes your organization’s knowledge, making it easy to find, document, and share content right where you work
Guru brings protocols, SOPs, and regulatory guidance into one searchable place, so your team can move faster and stay compliant.
From MSLs to CRAs, Guru gives everyone instant access to approved responses and guidance—no more chasing down internal experts.
Cut the overwhelm. Guru centralizes key onboarding content, FAQs, and process docs so new hires get confident, faster.
Built for the fast-paced world of pharma and clinical research, Guru combines the best of AI-powered search, wiki, and intranet features into one platform. Guru delivers instant, trusted answers sourced directly from your content—like study protocols, SOPs, regulatory guidance, and medical documentation—right within the tools your teams already use (including email, Slack, CTMS platforms, and document management systems). The result? Faster decision-making, audit-ready teams, and smoother collaboration across trials and functions.
Guru’s Knowledge Agents don’t just fetch generic search results—they deliver context-aware, tailored answers grounded in your verified data and information. By understanding who’s asking and what they need, Agents surface accurate, trial-specific insights from SOPs, study protocols, regulatory guidance, and more. Whether supporting CRAs, answering site questions, or managing amendments, Knowledge Agents deliver the right info, right in your workflow, so studies stay compliant and on schedule.
Whether pulling from connected data sources or storing critical study content in Guru, your team gets fast access to what they need. Guru’s intuitive editor makes it easy to document data and information while AI helps refine, translate, and clarify complex language for accuracy. Shared drafts and in-line comments keep clinical operations, medical affairs, and regulatory teams aligned—minimizing delays, miscommunication, and compliance risks across every phase of the trial.
Keep everyone on the same page with Custom Pages. Create dedicated spaces for study protocols, site training materials, regulatory updates, and trial timelines—all in one centralized location. Leaders can instantly share critical updates within existing workflows (like CTMS platforms, email, or Teams) and confirm they’ve been seen and acknowledged, resulting in fewer miscommunications, faster decision-making, and smoother clinical trial execution.
Users only see (and get AI-powered answers from) content they already have access to, keeping info secure.
Allow team members to document info instantly, with expert approval before team-wide publishing.
Automatically archive outdated guidance or protocol versions to keep teams working from the latest info.
Inaccurate content risks compliance—get automatic reminders to keep critical info verified and up to date.
Director of Data Strategy and Analytics
Advertising services | 501-1K employees
VP of GTM
Information technology and services | 201-500 employees
Human Resources and Support
iGaming Technology | 501-1K employees
Training Manager
Insurance | 201-500 employees
Marketing Director
Internet | 1-10 employees
Marketing Operations Manager
Mid-Market | 51-1000 employees
Marketing Manager
Marketing and Advertising
Customer operations
Banking | 5001-10,000 employees
VP of Sales
E-Learning Technology | 11-50 employees
Compliance Manager
Consumer Services
Marketing Manager
Marketing and Advertising
CEO
Broadcast Media
VP of Customer Success
Professional Training and Coaching
Customer Support Manager
Mid-market | 51-1000 employess
GM Finance & Accounting
IT services
Support Manager
FinTech | 50-200 employees
Head of HR
Writing and Editing | 11-50 employees
.avif)
.png)
