aria-planning

Generate structured regulatory project plans with phases, milestones, and dependencies.

Updated Feb 10, 2026

Search Tags:#planning #project management #dependencies #milestones #regulatory affairs #submission strategy

Ready to run

npx skills add https://github.com/henry-1981/Cowork-RA --skill aria-planning

💬 Prompt for ChatGPT / Claude Chat▼

Please help me install this Agent Skill.
Skill: aria-planning
Source: https://github.com/henry-1981/Cowork-RA/tree/main/aria/skills/planning
Command: npx skills add https://github.com/henry-1981/Cowork-RA --skill aria-planning

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill includes references (resource) components.

What problem does it solve?

This Skill automates the creation of structured regulatory project plans, including phases, milestones, and dependencies, based on pathway and estimation data.

Core Features & Use Cases

Phase-Based Planning: Generates plans with standard regulatory phases (Preparation, Testing, Documentation, Submission, etc.).
Dependency Mapping: Defines sequential, parallel, and milestone dependencies between tasks.
Multi-Region Strategy: Supports parallel or sequential submission strategies across different regulatory regions.
Use Case: After assessing a medical device's regulatory pathway and estimating timelines, use this Skill to generate a detailed project plan with key milestones and dependencies for submission to the FDA and EU.

Quick Start

Generate a regulatory milestone plan based on the provided pathway and estimation data.

Frequently Asked Questions about aria-planning

High-intent search queries and answers about installing and using this skill.

FAQPage Schema

How do I generate a regulatory submission plan with milestones and dependencies?▼

To generate a regulatory submission plan, you input pathway and estimation data to automatically create structured phases, milestones, and task dependencies. This produces a detailed project plan covering critical path analysis and standard regulatory phases like Preparation and Submission.

Can I plan multi-region regulatory submissions for FDA and EU simultaneously?▼

Yes, you can plan multi-region regulatory submissions using parallel or sequential submission strategies across different regions. The plan generates distinct milestones and dependencies tailored to each specific region's regulatory pathway requirements.

What input data do I need to create a regulatory project plan?▼

Creating a regulatory project plan requires pathway data and estimation data as inputs. The Skill utilizes this built-in knowledge and input data to map sequential, parallel, and milestone dependencies across standard regulatory phases.

How does dependency mapping work for regulatory project tasks?▼

Dependency mapping defines sequential, parallel, and milestone dependencies between regulatory tasks. It structures the project plan by linking phases like Documentation and Submission, ensuring tasks are properly sequenced for critical path analysis.

What's the best way to structure regulatory phases for a medical device submission?▼

The best way to structure regulatory phases is to use standard categories like Preparation, Testing, Documentation, and Submission. The plan automatically organizes these phases with corresponding deliverables and dependencies based on your specific pathway.

Does regulatory project planning support critical path analysis for submission timelines?▼

Yes, regulatory project planning supports critical path analysis by mapping sequential, parallel, and milestone dependencies. This analysis identifies the longest stretch of dependent tasks to accurately estimate submission timeline requirements.