Marketing, Brand & Commercial Teams

Create, adapt, and manage compliant micro-content across brands and markets without starting from scratch or entering MLR unprepared.
Create, approve, localize, and scale compliant medical micro-content faster - without adding MLR, design, or tech complexity.
Built by people who've lived life sciences timelines, reviews, and reality.
Qoolo is a micro-content authoring engine built for regulated teams who don’t have time to fight their tools.
Other content tools weren’t built for regulated industries. We are.
Qoolo helps life sciences teams build, approve, and scale compliant medical micro-content at speed without rebuilding workflows, adding friction, or losing control.
Create compliant micro-content in minutes, not weeks with a no-code builder made for life sciences. Build straight in your browser, no downloads, no hassle.
Drag. Drop. Done.
If you can use PowerPoint, you can build micro-content in Qoolo. Move fast with zero coding complexity.
Browser-based
No installs. No IT tickets. Qoolo runs entirely in your web browser and is always up to date.
Mobile-first
See your content exactly how HCPs will see it - no resizing, no shifting, no surprises.
Life sciences template library
Skip the blank page. Jumpstart content creation with ready to use templates built for realistic life sciences use cases.
Reimagined modular
Build once, reuse across brands, markets, and campaigns. Fewer edits, fewer errors.
Media library
Load once. Use always. Drag and drop your approved visuals, or create AI-powered assets on the fly.
Icon & shape library
Access 1,700+ pharma friendly icons and shapes to boost storytelling - searchable, ready to drop straight into your content.
AI that speeds things up
Use AI to generate visuals or get quick tips from our Qoolo Assistant to move faster and get your content to the next level.
Qoolo runs on our patent-pending micro-content platform, built for the realities of life sciences.
Qoolo is for teams who create regulated content.
Qoolo is designed for the people responsible for creating compliant micro-content in highly regulated life sciences.
Built for teams expected to move fast, stay accurate, and keep everything on brand while scaling across markets and brands.

Create, adapt, and manage compliant micro-content across brands and markets without starting from scratch or entering MLR unprepared.

Build accurate, scientific content that stays clear and readable even with complex references, footnotes, and endnotes built in from the start.

Deliver client-ready content within strict brand, compliance, and review requirements without custom builds or rework.
Why Qoolo?
Qoolo exists because life sciences teams outgrew iVAs, slide decks, PDFs, and everything in between. Most tools create files. Qoolo creates a compliant content system.
The usual way
vsThe Qoolo way
The usual way
Manual formatting that breaks every time content changes.
The Qoolo way
Built-in structure that keeps content consistent by design.

HCPs don’t have time to sit in offices and scroll through long medical content on a laptop. They steal moments. Between patients. In hallways. At home. In hospital cafeterias. On the move. Always on their phone.
That’s why Qoolo isn’t just about enabling the creation of mobile-friendly content. And it’s not just about making content short.
Qoolo is a mobile-first micro-content authoring platform for regulated life sciences teams, built to structure dense medical information and complex science into micro-content that works on small screens, without losing scientific rigor, context, or compliance.












Your next-gen mobile detail aid. Create short, focused, mobile-first micro-aids that sales reps can co-browse in-person, or send as a follow-up as self-guided mobile detail.
Mobile, micro-presentations for MSLs
Turn complex clinical updates into swipable micro-content your MSLs can co-browse or send via email or SMS - no laptops needed.
Article summaries
Turn scientific articles into bite-sized micro-content your MSLs or sales reps can share with doctors, or use to review key data.
QR-powered print
Swap out static handouts for smart, mobile-first content. Add a QR to printed materials - whether left at the clinic or handed out at a booth - and give HCPs instant access to the full experience on their phone.
Booth-To-Go experiences
Put your booth content on the mobile. Let HCPs visit your data or demos from their phone, during or after the event.
Conference highlights
Present conference highlights in quick and easy to navigate mobile story.
Micro-training on-the-go
Short, bite-sized training for sales and medical teams that can access on their mobile devices on-the-go. Create refreshers or onboarding flows in minutes and update anytime.
Interactive surveys and quizzes
Build quickly and capture on-the-go rep feedback, HCP preferences, or training comprehension. Fully mobile.
Regulatory documents
Get all of you regulatory documents available on the phone for easy access. Disclaimers, PI, ISI, abbreviated SmPC, loaded and auto-synced. One update applies across every mobile visual aid (MVA) and micro-content asset.
MLR-ready storyboards
Automatically generate MLR-ready storyboards.
Localized asset storyboards
Automatically generate storyboard for your localized asset.
Branded templates
Create once. Reuse everywhere. Have your brand safe mobile-first templates ready to build and launch fast.
"Neoqool" is a fictitious brand created by Qoolo for demonstration purposes only. See our Terms of Service for full details.
Build content fast, stay compliant, and keep everything on brand, without the dev time.
Qoolo makes building compliant, mobile-ready content as simple as drag, drop, and go. From branded product overviews to scientific materials to internal training documents, our no-code builder helps your teams move faster, stay compliant, and keep every asset on-brand.
Purpose-built for pharma. Not just another tool.
Most content platforms weren't made for the complexities of MLR review, strict brand guidelines, or the way field teams actually use content. Qoolo was. Created by people who've worked in pharma and know the struggles of timelines, compliance rules, and approval workflows. Qoolo streamlines the entire process - from first draft to final approval, helping you create content in minutes to hours, instead of weeks.
Trusted by marketing and medical teams across life sciences to create and publish faster - without reinventing workflows.

Set the rules once and scale your brand without starting over each time.
Qoolo gives you complete control over how your brand is applied across products, campaigns, and countries. From fonts and layouts to safety information and navigation flow, everything is set up through centralized workspace, so your team can move faster and your content can stay compliant by design.

References, footnotes, MLR review, handled from the start.
Qoolo is built for the regulatory demands of life sciences content. Whether you're preparing scientific, medical, or promotional materials, we help you get MLR-ready faster, with no manual formatting, and cleaner review documents.
Qoolo isn’t a closed system.
It fits into your existing ecosystem - connecting to the platforms your teams already use, from MLR and CRM to DAM and distribution. We integrate where it matters most, so workflows stay intact and teams keep moving fast.
Connect what you already use.
Integrate with tools like Veeva Vault, Salesforce, internal CRMs, DAMs, or MLR review platforms, without extra dev work. Think Qoolo can work for your team?

Scale global content, without doubling the work. In life sciences, localization is rarely about translation - it's updating ISIs, disclaimers, brand themes, and market-specific visuals, under tight timelines and strict review cycles. Qoolo builds localized content from the start, so global and local teams stay aligned, move faster, and keep compliance and design consistency intact.
When you need extra speed, you can use Qoolo's pharma-trained AI to generate first-draft translations in seconds - so local reviewers can refine and approve in one place, without develop support, endless file-swapping, or external vendors.

See what matters. Skip what doesn't. Take action faster.
In life sciences, analytics platforms often overwhelm you with noise or miss what actually drives impact. Qoolo takes a lean, focused approach that shows you the metrics that matter most, so you can optimize or adjust your content with confidence.
Qoolo helps you track what content gets viewed, where engagement drops off, and how users interact, without sifting through cluttered dashboards or messy spreadsheets.
Qoolo is built for life sciences timelines, reviews, and reality.
Qoolo is our flagship product and the foundational software layer of the Qoolo platform, built specifically for compliant, mobile-first medical micro-content in the life sciences industry. Qoolo helps teams create, manage, organize, brand, and analyze structured content in one centralized environment, making review-ready micro-content easier to build and scale across teams, brands, and markets.
Qoolo anchors a new category of software in life sciences, centered on medical micro-content rather than legacy document, deck, or eDetail formats. It also serves as the base for patent-pending platform capabilities and AI-enabled workflows that support faster, smarter, and more specialized ways of creating compliant content.
Qoolo is designed for life sciences teams responsible for creating, managing, and delivering content, including Marketing, Brand, and Commercial teams adapting compliant micro-content across brands and markets, Medical and MSL teams building accurate scientific content with references and endnotes built in, and agencies delivering client-ready content within strict brand and compliance requirements.
Qoolo is built so the people closest to the message can create structured, on-brand, and review-ready micro-content themselves, without depending on designers, developers, or heavy IT support.
Qoolo builds structure and review readiness into the content creation process from the start. References, endnotes, version history, and storyboard-ready outputs are handled as content is created, so materials stay organized, traceable, and ready for MLR and other review workflows.
Because content is built in structured, reusable units, teams update only what has changed instead of rebuilding entire assets. This reduces manual rework, maintains accuracy and consistency, and makes compliant micro-content easier to manage across brands, markets, and use cases.
Qoolo supports existing MLR review workflows, not replaces them. Teams continue using their established approval environments while using Qoolo to prepare structured, review-ready content more efficiently before it enters formal review.
Qoolo generates storyboard-ready outputs and keeps references, endnotes, and content structure organized from the start, which reduces screenshots, manual formatting, and rework. Where needed, Qoolo can also connect into third-party review environments such as Veeva Vault, depending on setup and implementation scope.
Qoolo manages global and local content from a centralized workspace, so teams maintain master materials while adapting content for different markets, regions, or use cases. Teams update only the parts that need to change rather than rebuilding content from scratch, which preserves consistency while allowing local flexibility.
Because content is structured and reusable, layouts, references, and core content logic stay aligned across versions. Qoolo also supports faster localization workflows, including AI-enabled translation support and market-specific adaptation, so global-to-local teams move efficiently while staying within brand and compliance expectations.
Qoolo keeps teams on-brand by giving them a structured environment where content is created within approved visual and content rules from the start. This keeps layouts, styling, and content presentation consistent across products, campaigns, and regions without manual design checks or rework.
Whether content is for a global launch, local market adaptation, advisory board materials, or conference use, Qoolo helps teams move faster while keeping content aligned with brand expectations.
Once content is live, Qoolo gives teams visibility into how content is performing and how audiences are engaging with it. Teams monitor KPIs such as Total Views, Average Time, and Completion Rate, so they understand not just whether content was opened, but how it was used.
Qoolo's Analyze capabilities also include Unique Views and per-screen drill-down within each piece of content, with filters for time period, geography, and channel. Tracking is anonymous by default, so teams see what is resonating, where engagement drops off, and where updates may be needed, without added privacy review.
No. Qoolo is browser-based, so teams access it without local installations, downloads, or heavy IT involvement. Both larger organizations and leaner teams get started quickly and begin creating, managing, and using content in one centralized environment.
For enterprise customers, Qoolo also supports integrations with existing systems such as MLR platforms, CRM environments, or other internal tools, depending on setup and implementation scope. For teams that do not need that level of integration, Qoolo works effectively as a standalone platform.
Yes. Qoolo supports both internal and external use cases in the same platform. Teams use it for internal training, onboarding, field enablement, advisory board preparation, and other organizational workflows, as well as for external HCP engagement before, during, and after meetings, events, or follow-up activities.
The same structured content, brand logic, and compliance-ready workflows support different audiences and moments, so teams do not duplicate effort across separate tools.