Comprehensive medication safety review system providing real-time analysis of drug-drug interactions, contraindications, allergy risks, and dosing optimizati...
FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QSR (21 CFR 820) compliance, HIPAA assessments, and dev...
Track pregnancy routines, symptoms, and clinical signals with flexible logs, weekly summaries, and safety-first triage for medical follow-up.
Extract clinical phenotypes and medication entities from user-provided text using PhenoSnap, producing a timestamped JSON output.
Zoom/Teams/Meet 远程会议AI助手。Use when: user asks to join a meeting, monitor a meeting, record a meeting, assist in a medical consultation, help doctor-patient co...
Compare health insurance plans, estimate total yearly costs, and choose coverage that fits medical usage, prescriptions, and financial risk.
EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Covers Ann...
ISO 13485 Quality Management System implementation and maintenance for medical device organizations. Provides QMS design, documentation control, internal aud...
Medical device risk management specialist implementing ISO 14971 throughout product lifecycle. Provides risk analysis, risk evaluation, risk control, and pos...
Label-backed medication answers with citations and traceable IDs. RxCUI/NDC/set_id, key label sections, optional recalls/shortages/FAERS/interactions.
Converts complex medical abstracts into plain language summaries for patients, caregivers, and the general public. Ensures readability while maintaining scie...
Health data management system for tracking blood pressure, heart rate, exercise, and medication. Use when: (1) recording daily health metrics like blood pres...
Curated skill bundle for medical device companies, digital health startups and pharma R&D teams. Activates the firm pyramid with RA (Regulatory Affairs), Cli...
Helps creating FHIR conforming questionnaire definitions from plain requirement ideation docs. Contains scripts to look up LOINC and SNOMED CT codes for medical conditions, findings, observations, med
ISO 13485 internal audit expertise for medical device QMS. Covers audit planning, execution, nonconformity classification, and CAPA verification. Use for int...
Document control system management for medical device QMS. Covers document numbering, version control, change management, and 21 CFR Part 11 compliance. Use...
Search and order pharmacy products from apohealth.de via apo-cli. Use for medication search (by name or PZN), product details, category browsing, and cart management. Trigger when the user mentions Ap
Assist in structuring medical-tech bootcamps, crafting health-tech content, and analyzing Sharia-compliant trades with Python and data-driven insights.
CAPA system management for medical device QMS. Covers root cause analysis, corrective action planning, effectiveness verification, and CAPA metrics. Use for...
Patiently AI simplifies medical documents for patients. Takes doctor's letters, test results, prescriptions, discharge summaries, and clinical notes and expl...