Med-Researcher Guide
Multi-agent system for biomedical literature review and synthesis
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Multi-agent system for biomedical literature review and synthesis
Comprehensive computational validation of drug targets for early-stage drug discovery. Evaluates targets across 10 dimensions (disambiguation, disease association, druggability, chemical matter, clinical precedent, safety, pathway context, validation evidence, structural insights, validation road...
Comprehensive patient stratification for precision medicine by integrating genomic, clinical, and therapeutic data. Given a disease/condition, genomic data (germline variants, somatic mutations, expression), and optional clinical parameters, performs multi-phase analysis across 9 phases covering ...
Act as a medical tutor to answer surgery questions and rationalize multiple-choice options based strictly on Schwartz Principles of Surgery 11e, requiring explicit citations.
Simulate a gastroenterology professor to test a GP or medical student on medical topics. Administer questions (one-by-one or as an exam), evaluate clinical reasoning, and provide a numerical grade out of 100.
Generates a comprehensive medical essay covering anatomy, histology, physiology, biochemistry, pharmacology, and pathology. The output must be in Notion-style Markdown format, include emojis for visual appeal, and provide detailed explanations for each section.
Senior QMS Audit Expert for internal and external quality management system auditing. Provides ISO 13485 audit expertise, audit program management, nonconformity identification, and corrective action verification. Use for internal audit planning, external audit preparation, audit execution, and a...
Senior Risk Management specialist for medical device companies implementing ISO 14971 risk management throughout product lifecycle. Provides risk analysis, risk evaluation, risk control, and post-production information analysis. Use for risk management planning, risk assessments, risk control ver...
Expert AI auditor for Medical Device (SaMD) compliance, IEC 62304, and 21 CFR Part 820. Reviews DHFs, technical files, and software validation.
Medical device cybersecurity risk assessment skill per FDA premarket and postmarket guidance
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