Expert-thinking subagents for molecular & cell biology: genetics, genomics, omics, biochemistry, biophysics, microbiology, immunology, virology, and structural/synthetic/systems biology.
63 agents
Clinical decision support, clinical/case/trial reports, treatment plans, and ISO 13485 QMS docs.
Plugin sci-clinical-research from marketplace plugin-place in galeep/plugin-place. Commands read from the repo's manifest — today.
analytical-method-validationPlan, execute, and document validation, verification, and transfer of analytical procedures under the governing framework - ICH Q2(R2) and Q14, USP <1220>/<1225>/<1226>, ICH M10 bioanalytical, CLSI EP, or ISO/IEC 17025. Use for HPLC, LC-MS/MS, GC, CE, ICP-MS, dissolution, qNMR, qPCR, NIR, and ligand
clinical-decision-supportPrepare and validate research-only clinical decision-support evaluation, evidence-profile, cohort, survival, biomarker/model, privacy, and governance artifacts. Use for aggregate or synthetic research documentation and traceability—not patient care or live clinical operation.
clinical-reportsCreate safety-bounded draft structures and run local deterministic checks for clinical case, diagnostic, trial, safety, and aggregate research reports. Use only with synthetic, de-identified, or aggregate inputs and verified source-fact manifests; every output requires qualified review.
iso-standards-readinessPrepares and structurally reviews readiness evidence for ISO management-system and laboratory-competence standards - ISO 13485 medical device QMS, ISO 14971 device risk management, ISO/IEC 17025 testing and calibration laboratories, and ISO 15189 medical laboratories. Use when organizing declared sc
pkpd-modelingPharmacokinetic and pharmacodynamic modelling and simulation - non-compartmental analysis, compartmental and population PK, PK/PD and exposure-response, TMDD, PBPK orientation, bioequivalence, allometric scaling and first-in-human dose, drug interaction prediction, and Bayesian therapeutic drug moni
relsa-severity-assessmentMultivariate severity assessment and humane endpoint prediction for laboratory animal studies using the RELSA (RELative Severity Assessment) score and ARIMA-based foRcast forecasting. Use when combining welfare readouts — body weight or weight loss, body temperature, clinical or nesting scores, biom
treatment-plansFormat and structurally validate local treatment-plan documentation after clinical decisions have already been supplied and verified by authorized licensed professionals. Use for source traceability, clinician-authored intervention records, goals and checkpoints, shared-decision records, reconciliat
Expert-thinking subagents for molecular & cell biology: genetics, genomics, omics, biochemistry, biophysics, microbiology, immunology, virology, and structural/synthetic/systems biology.
63 agents
Expert-thinking subagents for clinical medical specialties: cardiology, oncology, radiology, pathology, neurology, surgery, anesthesiology, pharmacology, and related fields.
54 agents
Expert-thinking subagents for chemistry: organic, inorganic, physical, analytical, electrochemistry, catalysis, spectroscopy, mass spectrometry, and crystallography.
48 agents
Expert-thinking subagents for mechanical, civil, chemical, aerospace, and process engineering: fluid dynamics, structures, manufacturing, thermodynamics, and reliability.
48 agents
Expert-thinking subagents for earth, environmental, ocean, and atmospheric science: geology, geophysics, climate, oceanography, hydrology, remote sensing, and sustainability.
46 agents
Expert-thinking subagents for organismal, ecological, and evolutionary biology: zoology, botany, physiology, taxonomy, phylogenetics, conservation, and marine/field biology.
43 agents
Evidence-backed BioPharma research workflows over Maven Bio's drug, trial, company, and deal knowledge graph. Skills for competitive pipelines, indication landscapes, asset profiles, deal and financing activity, and evidence synthesis grounded in FDA, SEC, clinical, and press sources. Requires a Maven Bio account.
16 skills · 1 agent · 1 MCP server
14 regulatory affairs & quality management skills for HealthTech/MedTech: ISO 13485 QMS, MDR 2017/745, FDA 510(k)/PMA, GDPR/DSGVO, ISO 27001 ISMS, CAPA management, risk management, clinical evaluation, SOC 2 compliance.
21 skills
Sets up the clinic, onboards students, runs structured intake, tracks deadlines with malpractice-aware caution, and hands off cases at semester end — built within ABA Formal Op. 512.
16 skills · 5 MCP servers
General life-sciences research workflows with query routing, evidence synthesis, and optional parallel subagent analysis across genetics, omics, biology, chemistry, structure, clinical evidence, and public dataset discovery.
50 skills
De-identify PHI, run clinical NER, export FHIR, evaluate with leakage gates, and the healthcare workflows around them.
74 skills
Operator-grade OpenEvidence pack with 24 source-grounded skills for clinical evidence review, safe adoption, privacy, security, and product workflow governance.
24 skills
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