Clinical Trials
Track clinical trial progress, regulatory submissions, and milestone timelines. Built for biotech founders navigating FDA, EMA, and global regulatory pathways. This is still a catalog page: it shows the available skills, but the surrounding product and solution context lives elsewhere.
Skills
Clinical Trial Status
@clinicalGet current status of your clinical trials. Tracks phase, enrollment, sites, and key milestones.
Examples
@clinical what's the status of our Phase 2?@clinical how many patients enrolled?@clinical when is our next data readout?@clinical summarize trial progress for the boardFDA Pathway
@fdaTrack FDA submissions, meetings, and regulatory pathway. Covers IND, NDA, BLA, 510(k), and breakthrough designations.
Examples
@fda when did we submit our IND?@fda what's needed for our pre-NDA meeting?@fda do we qualify for breakthrough designation?@fda timeline to approvalEMA Pathway
@emaEuropean regulatory tracking. PRIME designation, scientific advice, MAA submissions.
Examples
@ema PRIME eligibility check@ema compare FDA vs EMA timelines@ema what's our EU regulatory strategy?Trial Design Review
@trial-designAnalyze trial design, endpoints, sample size, and comparator selection. Cross-reference with similar approved trials.
Examples
@trial-design review our Phase 3 protocol@trial-design what endpoints did competitors use?@trial-design is our sample size sufficient?@trial-design adaptive design optionsNeed more than the pack?
Bridge back to product surfaces, use cases, and resources
Use the catalog to pick a capability. Use the rest of the site when you need the broader product map, the workflow story, or detailed guidance.
Platform overview
Use the platform overview when you need the system map before choosing a capability.
Use cases
Use /solutions when the question is about a workflow or use case rather than a specific capability.
Platform surfaces
Use /platform when you already know the surface you want to work in.
Resources hub
Use /resources for help, developer docs, security, and higher-level guidance around the capability layer.