proompts

Table of Contents

Business

Scenario-Based Clinical-Trial Cash-Flow Forecast
Competitive-Bid Pricing & Margin Optimizer
Regulatory-Risk & ESG Impact Dashboard Builder
Emerging-Market Opportunity Scan
Market-Intelligence Radar
Rapid Proposal Builder
RFP Executive-Summary Generator
90-Day Pipeline Health & Next-Best-Action Review
Competitor-Positioning Brief
Strategic Workforce and Talent Acquisition Plan
Clinical-Trial Budget and Burn-Rate Dashboard
GCP and GDPR Training Compliance Risk Report
Market Landscape & Trend Analysis
Target Segment & User Needs Assessment
Regulatory & Commercial Barrier Mapping
Market Report Executive Summary
Build an Audit-Ready Site-Payment Schedule
Sunshine Act and FMV Compliance Check
Payment-Process Risk Assessment and Mitigation
Investigator-Site Payment Forecast
Payment Reconciliation and Discrepancy Report
Global Regulatory and Tax Matrix for Site Payments

Clinical

Real-Time Adjudication Visibility Dashboard
Source Document and Endpoint Checklist
Analyze Adjudication KPIs
Monitoring-Visit Report Generator
Investigator Follow-up Email & Action-Item Tracker
Risk-Based Monitoring (RBM) Plan Builder
Discrepancy Detection & Query Log Generator
Draft a Data Management Plan Section
Edit-Check Specification Builder for New eCRF Fields
Unified Data Cleansing
Regulatory Gap Analysis
Data Architecture Blueprint
Clinical ETL Mapping Spec
Clinical ETL Transformation QC
Clinical ETL Pipeline Review
Phase II Oncology DMP
Decentralized Trial Risk Matrix
SOP Gap Analysis
Architect the Integration Blueprint
Data Mapping and Transformation Playbook
Regulatory and Validation Checklist
Patient-Centric BYOD ePRO Workflow
Optimize ePRO Form Design
ePRO Adoption Plan for Sponsors
CRF Shell Generator
CRF Quality Auditor
CDASH Mapping & Completion-Guide Assistant
Imaging Charter Draft
Site Upload QC and Query Generator
Central Reading Paradigm Design
Regulatory Imaging Charter Generator
Image Acquisition QC Workflow Blueprint
Regulatory Imaging Data Package
Risk-Based Site Performance Dashboard
CAPA Plan Builder for Monitoring Findings
Monitoring Visit Report (MVR) Quality Critique
Clinical-Trial Protocol Creator
Ultimate SOP Architect
Protocol Reviewer and Gap-Analysis Coach
Protocol Section Refinement
Design a Patient-Centered Randomization Scheme
Forecast Site-Level Drug Supply & Resupply Strategy
Create a Risk-Based Monitoring & Mitigation SOP for RTSM
Clinical Safety Synopsis for EU MDR CER
FDA MDR/MDV Adverse-Event Narrative
Post-Market Safety Signal Trending
Site Landscape Mapping & Prioritization
Tailored Feasibility-Questionnaire Builder
Personalized Investigator-Outreach Email Generator
Protocol Optimization and Risk Simulation
AI-Powered Site and Recruitment Strategy
Compliance and Data Quality Monitoring Plan
Adaptive Recruitment and Retention Strategy
Portfolio-Level Clinical Operations Roadmap
Risk-Based Monitoring and Quality Plan
Patient Recruitment and Diversity Acceleration Plan

General

Management

Accelerate Patient Recruitment & Retention
Digest the Latest Regulatory Updates Affecting My Protocol
Portfolio KPI Dashboard Brief
Strategic Market Foresight and Action Plan
Crisis-Management Playbook Generator
Executive-Ready Brief and Talking Points
Digital Transformation Roadmap for Clinical Operations
Strategic Market and Competitor Radar
Strategic Growth Roadmap
Strategic Portfolio Prioritizer
FDA-Aligned AI Governance Framework
Emerging-Science Horizon Scan
Executive Trial-Health Dashboard
Investor and Board Narrative Builder
Quarterly Innovation Radar for Decentralized and Hybrid Trials
Regulatory and Competitive Intelligence Briefing
Trial-Design Optimisation Memo
Hosting Cost Reduction ToT Plan
Strategic Consultant SWOT
Strategic Alignment and Innovation
Operational Excellence Communication Framework
Leadership Reflection and Culture
90-Day Biostatistics Onboarding Plan
Clinical Trial Protocol Compliance Review
Pharmacovigilance Safety Signal Prioritization
AI-Enhanced RBM Action Plan
Rapid Process Diagnostic & Lean Improvement Plan
Inventory & Demand-Planning Simulation
KPI Dashboard & Monthly Ops-Review Pack
CRO Trial-Performance KPI Dashboard Blueprint
Operational Excellence & Risk Sweep
360° Operational KPI & Benchmark Review
Rolling Resource & Capacity Forecast
Study Start-Up Checklist & Timeline
Multistudy Resource & Capacity Forecast Plan
Proactive Risk Heat-Map for Decentralized & Virtual Trials
Quarterly CRO KPI Executive Brief
Weekly Operations KPI Snapshot
Action-Oriented Meeting Minutes & Tracker
Fair-Market-Value Budget Negotiation Brief
Forward-Looking Resource & Capacity Forecast
Risk-Based Vendor Performance Improvement Plan
Project Charter and Scope Definition
Comprehensive Risk Register and Mitigation Plan
Weekly Executive Status Report
Detailed Project Blueprint and Timeline
Risk and Pre-Mortem Analysis
Status Update and Task Prioritization
Clinical-Trial Timeline and Risk Radar
Portfolio Resource and Budget Forecast
Cross-Study Operational Risk Heat Map and Mitigation Plan
Sponsor-Ready Monthly Status Brief
Executive Sponsor Briefing Deck Outline
TMF Gap-Analysis and Audit Readiness Check
Neutral Scrum Retrospective Facilitator
Rollout Risk Matrix
Draft a GLP-Compliant Study Protocol
Audit Raw Data and Draft a CAPA Summary
Generate an Executive Summary for the Final Report
Interim Results Executive Brief
Statistical Analysis Plan Draft Builder
Data-Quality Risk Heat Map

Meta

Master Ultrameta Prompt Architect
Meta Prompt Architect
Prompt Engineer Template
Task Prototyper
Worker Prompt
AGENTS.md Checklist Generator
AI Coding Agent Plan Generator
Comprehensive Task Template
Prompt Engineer Fact Checker
PromptCrafter GPT
README Generator

Regulatory

Regulatory Radar & Impact Report
Compliance Gap & Risk Matrix
Quality-Improvement RCA & Action Plan
eTMF Compliance Gap Analysis
Regulatory-Landscape Radar
CAPA Plan Generator
Inspection-Readiness Drill (CAPA Builder)
Integrated Submission Strategy Coach
Risk-Based Quality Management Plan
510(k)/De Novo Pre-Submission Strategy
EU MDR Technical-Documentation Gap Assessment
Regulatory-Change Impact Analysis
Strategic Regulatory Pathway Plan
Compliance Gap Assessment
IND Readiness Gap Analysis & Filing Road-Map
IVDR Performance-Evaluation Plan Blueprint
RA/QA Integrated Quality System Audit
Dual MDR / IVDR Conformity-Assessment Roadmap
IVD Performance Study Compliance Review
21 CFR 820 / QMSR Gap-Analysis & Remediation
Regulatory Filing Draft Builder
Prompt-Writing Best-Practice Checklist
Literature & Regulatory Gap Analysis

Scientific

Risk Assessment Expert
Biological Safety Plan Developer
Regulatory Submission Support
Biological Evaluation Plan Builder
Comprehensive Biocompatibility Test Matrix
Chemical Characterization & TRA Work Plan
Hands-On Procedure Coaching
Simulated Clinical Scenario Debrief
Objective Skills Assessment
Statistical Analysis Plan Generator
Time-to-Event Analysis Coach
Peer-Review Checklist for Manuscript Methods
Universal Template-Table Prompt
Dual-Language Figure Prompt
QC Listing & Cross-check Prompt
Study Design and Statistical Approach
Inclusion/Exclusion, Endpoints & Sample-Size Deep Dive
Adaptive Design & Interim Monitoring
Phase II/III SAP Skeleton
Sample-Size & Randomization Strategy
FDA Missing-Data Query Response
Submission-Ready Statistical Analysis Plan
Generate & QC Submission-Ready TLFs
Design the Study
Interpret the Chemistry & Assess Risk
Write the Regulatory Summary
Bioburden Testing SOP
EO Sterilization Validation Protocol
Endotoxin Control & 510(k) Risk Plan
Design a Robust Preclinical Pathology Study Protocol
Evaluate Device–Tissue Interface Findings
Prepare Pathology Slides and Reporting Plan
Sterility-Validation Protocol Builder
Regulatory Gap-Analysis Comparator
EtO Sterilization Process FMEA

Technical

Product Brief Template
Project Brief for Epic
Technical Implementation Plan
Coding Session Guidelines
Project Review Checklist
Project Memory Notes
To-Do List Template
E2E Test Discovery Template
Folder and Module Organization
RequirementsBot Prompt
Reflexion Agent Bug Patch
DRY Codebase Analysis
Maintainability Codebase Analysis
SOLID Codebase Analysis
Project Init & Skeleton (OpenAI Codex)
Codebase Testing Plan
Tooling, Linting & Quality Gates (OpenAI Codex)
Continuous Integration & Delivery (OpenAI Codex)
Documentation & Developer Onboarding (OpenAI Codex)
Refactoring Suggestions (OpenAI Codex)
Architecture Flow Q&A (OpenAI Codex)
Security Vulnerability Hunt (OpenAI Codex)
Code Review Assistant (OpenAI Codex)
Targeted Test Generation (OpenAI Codex)
Bug Finder & Fixer (OpenAI Codex)
UI Tweak & Verification (OpenAI Codex)
Design.md Template
AI Email Assistant Go/No-Go Vote
Forge - Script Reliability Agent
Atlas Documentation Specialist
Repository Foundation & Developer Experience Analysis
Codebase Quality & Maintainability Analysis
Dependencies & Security Posture Analysis
Testing, Configuration, and Automation Analysis
Documentation and Repository Structure Implementation
Code Formatting, Linting, and Refactoring Implementation
Security Hardening and Dependency Management Implementation
Test Suite Enhancement and CI Pipeline Implementation
CSR Results and Safety Section
Investigator’s Brochure Summary of Changes
SAE and Unanticipated Problem Reporting SOP
E2E Test Discovery Template
Design Verification Test Plan
Human Factors Validation Study Protocol
Risk-Based Test Case Suite

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