On-Demand Automation for Clinical, Regulatory and Cosmetics Data
Four global data domains. One platform. Regularly refreshed.
Vasl AI runs on-demand automation that aggregates and regularly refreshes data from global data repositories, bringing clinical trial, pharma regulatory, medical device regulatory, and cosmetics ingredient information together into one unified workspace, so your team spends less time hunting across sources and more time acting on reliable information.
No credit card required
Global Clinical Trials
Regularly refreshed
Pharma Regulatory
Regularly refreshed
Medical Devices
Regularly refreshed
Cosmetics Ingredients
Regularly refreshed
Four global databases, one platform
Vasl AI is built around on-demand automation. Instead of manually checking dozens of registries and agency sites, our platform pulls the data in, structures it, and keeps it regularly refreshed, so you have a current picture without the manual legwork.
It's a single system that aggregates records from sources like ClinicalTrials.gov, WHO ICTRP, EMA, MHRA, PMDA, Health Canada, TGA, and NMPA, so research, regulatory, and commercial teams can search one place instead of dozens of agency portals.
Global Clinical Trial Database
Vasl AI aggregates data from publicly available and licensed clinical trial registries around the world, covering sponsors, phases, indications, sites, and status, into one searchable, standardized view for your research and commercial teams.
Regularly refreshedPharma Regulatory Database
This service tracks approvals, submissions, labeling changes, and agency actions from regulatory bodies including EMA, MHRA, PMDA, and Health Canada, so your regulatory affairs and submission-tracking teams can follow a product's journey without switching between agency portals.
Global agency coverageMedical Device Regulatory Database
This service covers device clearances, registrations, post-market surveillance, recalls, and safety data across global markets, giving device makers a single place to check regulatory status and compliance history before it becomes a bottleneck.
Clearances & recallsCosmetics Ingredients Database
This service brings together ingredient-level data aggregated from public and licensed cosmetics regulatory sources, including restrictions and regulatory status by region, helping formulation and compliance teams check an ingredient before it ever reaches a label.
Region-by-region statusAutomation, not manual work
Every service on Vasl AI is powered by the same automation engine, built to aggregate, clean, and refresh data so your team spends less time collecting information and more time acting on it.
Aggregates from global repositories
Vasl AI connects to registries such as ClinicalTrials.gov and WHO ICTRP, regulatory agencies including EMA, MHRA, PMDA, Health Canada, TGA, and NMPA, plus cosmetics ingredient sources like CosIng, pulling everything into one platform instead of leaving it scattered across dozens of sites.
Refreshes data on demand
Rather than relying on a fixed update schedule, our automation checks source repositories on demand, so the records you're viewing reflect what's actually current, not what was current last quarter.
Standardizes everything into one view
Raw data from different agencies and registries rarely uses the same format. Vasl AI cleans and standardizes it before it reaches your dashboard, so you're comparing like with like across all four databases.
Puts it on a single platform
Clinical trials, pharma regulatory, medical devices, and cosmetics ingredients all live under one login and one dashboard, so switching between data domains takes a click, not a new subscription.
Built for how your team searches
Natural-language search and role-based dashboards mean research, regulatory, and commercial users each find what they need quickly, without learning a new query language.
Export-ready, always
Every service comes with downloadable charts, tables, and summaries, so what you find in Vasl AI is ready to drop straight into a report or a board update.
What services does Vasl AI provide?
What does the global clinical trial database cover?
What is included in the pharma regulatory database?
What does the medical device regulatory database include?
What is in the cosmetics ingredients database?
How often is the data refreshed?
Can I access all four databases on one plan?
How do I get started with Vasl AI's services?
Data on this page is aggregated from public and licensed regulatory and clinical trial sources. While we work to keep it accurate and regularly refreshed, please verify critical regulatory decisions directly with the relevant authority.
Old way vs. Vasl AI
Clinical operations, regulatory affairs, and CRO teams typically piece this together by hand. Here's what that looks like next to an automated, single-platform approach.
| Traditional method | Vasl AI |
|---|---|
| Manual search across agency sites (EMA, MHRA, PMDA, Health Canada) | Automated aggregation into one platform |
| Multiple portals and logins per registry or database | One login, one dashboard, four data domains |
| Weekly or monthly manual refresh cycles | On-demand and scheduled automated updates |
| Inconsistent formats across sources | Standardized, comparable records |
| Manual report building for stakeholders | One-click exports and executive summaries |
Key Takeaways at a Glance
- Vasl AI runs on-demand automation across four global data domains: clinical trials, pharma regulatory, medical device regulatory, and cosmetics ingredients.
- Data is aggregated from public and licensed sources such as ClinicalTrials.gov, WHO ICTRP, EMA, MHRA, PMDA, Health Canada, TGA, and NMPA.
- Records are standardized and regularly refreshed, on demand and on a schedule, instead of being updated manually.
- All four databases live under a single login, with role-based dashboards for research, regulatory, and commercial teams.
- Every service supports one-click exports, so findings are ready for reports and board updates without reformatting.
Try all four databases free for 30 days
Get hands-on with the full Vasl AI platform and see how much time your team gets back when the data comes to you, refreshed and ready.
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