Results for “clinical”

Design prospective clinical studies by selecting and classifying endpoints, estimating sample size and power for two-arm designs, and scoring study plans for feasibility with phase-gate decisions.

Generates a strategic NIH funding overview as an editable .docx file, including research positioning analysis, institute mapping, targeted grant discovery, and strategic recommendations for clinical researchers.

Simulates meiotic recombination to produce offspring genomes from parent pairs, modeling Mendelian segregation, de novo mutation, sex determination, trait inference, and clinical evaluation against a disease registry.

Audits medical LLM benchmarks across five lifecycle phases using 46 medically tailored criteria to assess clinical relevance, data integrity, safety-critical capabilities, validity, and governance.

Use this first, before any writing, to stress-test whether a clinical study clears NEJM's bar — practice-changing clinical impact, methodological rigor, and generalizability. Decides NEJM vs Lancet/JAMA vs a specialty journal.

Produces academic papers, literature reviews, grant proposals, and clinical reports with LaTeX formatting and verified citations, using research-lookup and parallel-web skills.

EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Covers Annex VIII classification rules, Annex II/III technical files, Annex XIV clinical evaluation, and EUDAMED integration.

Classify medical devices under EU MDR 2017/745, build technical documentation, plan clinical evaluations, and manage post-market surveillance and EUDAMED integration.

Generate concise (3-4 page) medical treatment plans in LaTeX/PDF format across all clinical specialties, with SMART goals, evidence-based interventions, and HIPAA compliance.

Guides DPIA for health and medical data processing covering Art. 9(2)(h)-(j) exemptions, HIPAA crosswalk for transatlantic operations, clinical trial data protection under EU CTR 536/2014, and genetic data specifics under Art. 9(1). Activate for healthcare systems, clinical research, health apps, or medical device data. Keywords: health data, DPIA, Art. 9, clinical trial, genetic data, HIPAA, medical records, special category.

A reflective tarot draw for emotional support (presence-first, non-clinical, non-predictive).

Clinically informed wisdom companion blending psychology and philosophy into a structured thinking partner

Clinically informed wisdom companion blending psychology and philosophy into a structured thinking partner

Clinically informed wisdom companion blending psychology and philosophy into a structured thinking partner

Draft an internal legal research memo for the supervising attorney with verified authority and flagged open questions.

Clinically informed wisdom companion blending psychology and philosophy into a structured thinking partner

Draft a legal document — a pleading, motion, brief section, or contract clause — with verified citations, flagged assumptions, and mandatory supervisor review before filing.

Clinically informed wisdom companion blending psychology and philosophy into a structured thinking partner

Onboard a new clinic student onto a matter and the clinic's systems fast, with supervision and confidentiality from day one.

Evidence-based health research using tiered trusted sources with GRADE-inspired evidence ratings. Integrates Apple Health data for personalized context. Use when user asks health, nutrition, exercise, sleep, or wellness questions.

Clinically informed wisdom companion blending psychology and philosophy into a structured thinking partner

Produce a concise matter status update for the supervising attorney or case rounds, separating settled facts from open questions.

Query the ClinPGx API for pharmacogenomic gene-drug data, clinical annotations, CPIC guidelines, and FDA drug labels.

Expert in human behavior, personality theory, motivation, and cognitive patterns — builds psychologically credible characters and interactions grounded in clinical and research frameworks

Queries the ClinPGx REST API for pharmacogenomic gene-drug data, clinical annotations, CPIC guidelines, and FDA drug labels, generating markdown reports with CSV tables.

Filters and prioritizes compound libraries in drug discovery using drug-likeness rules, structural alerts, complexity metrics, and a query language.

Clinical copy-editor that reviews text for communication issues. Use when user says review for prose or improve the prose

NIH grant research skill for clinical researchers. Grill-me intake (research idea + career stage + preliminary data + environment + submission posture + known institute targets) locks down the funding strategy before any search runs. Runs a 5-facet Consensus positioning analysis (with draft Significance/Innovation language), maps the research to the right NIH institutes and study sections via RePORTER, finds NOSIs and funded overlap, and produces an editable Word document (.docx) with budget/scope-aware mechanism recommendations, submission timelines, and a mandatory program officer recommendation. Use when the user asks about research funding or makes any grant-related request (e.g., 'grants for [topic]', 'find grants for my research idea', 'what grants match my research', 'help me find NIH funding', 'grant opportunities for my research'). NIH-only scope — non-NIH funders (PCORI, DOD CDMRP, VA, foundations) are out of scope and flagged at intake.

Clinical copy-editor that reviews text for communication issues. Use when user says review for prose or improve the prose

Create patient intake forms with history and screening. TRIGGERS - Use when user needs help with intake-form related tasks.