The all-in-one AI plugin for Biomedical Engineers

Skills for biomedical engineers 10

• office meeting notesTurns a design review transcript into decisions and action items, like who owns the next biocompatibility test.
• process risk assessment assistantBuilds FMEA and risk registers for device manufacturing, for example scoring seal failure risk on a catheter line.
• healthcare data analysis assistantFinds patterns in patient and device data, like flagging infusion pumps with rising battery fault rates.
• agency summarize meetingWrites formal minutes with date, participants, topic, decisions, and actions, ready for the quality file.
• meeting distiller proCleans up messy notes into actions, decisions, and follow-ups, like a supplier call about component delays.
• agency ra qm skillsRoutes you to the right regulatory skill, whether ISO 13485, EU MDR, FDA, ISO 14971, or CAPA.

Plus a start-here assistant, the prompt library and the app builder, and for members the daily brief.

Ready-made prompts 26

• Clinical Requirements & Needs3 prompts, like Summarize Clinician Interviews Into Requirements
• Explaining Devices & Procedures3 prompts, like Explain Device To Clinician
• Troubleshooting & Technical Support3 prompts, like Diagnose Device Error From User Report
• Design & Test Documentation3 prompts, like Create Detailed Prototype Test Plan
• Regulatory & Risk Compliance3 prompts, like Summarize Applicable FDA Guidance
• Data Analysis & Device Improvement3 prompts, like Prioritize Device Improvements From Feedback
• Collaboration & Project Communication5 prompts, like Prepare A Design Review Agenda

Apps you can build with AI 3

• Medical equipment downtime coordination networkBuild this to cut the delay between a scanner going down and authorized maintenance arriving, with status visible to everyone. Demo included.
• Product requirements serviceBuild this to keep device requirements tied to customer evidence and open questions, so nothing gets assumed. Demo included.
• Customer feedback insight and prioritization workspaceBuild this to turn scattered clinician and patient feedback into ranked, source-backed design priorities. Demo included.

AI agents 12

In the download. An agent runs a whole recurring task for you, step by step, and asks you before anything important. Ask your AI: "Run the Product Requirement Change Impact Agent". Each one also has a guided set-up with sample data on its page.

• Product Requirement Change Impact AgentEvery requirement change reaches all linked tests, docs and teams.
• User Test Prototype Iteration AgentTurn test observations into ranked problems and verified changes for the next prototype.
• Lab Meeting Action Follow-up AgentMake sure every action item from a meeting has an owner, a date and a recorded outcome.
• Usability Study Use Error Tracking AgentEvery observed use error, close call and difficulty is traced to a hazard and a mitigation before the report.
• Device Software Change Assessment AgentA documented impact assessment and test plan for each software change, with no requirement left untested.
• Post-Market Surveillance Review AgentA monthly, documented review of external events with relevant new hazards turned into drafted risk file updates.
• Hardware Test Plan and Results AgentA repeatable test plan with recorded, comparable results for every build
• Hardware Compliance Pre-Check AgentA design checked against certification requirements before it goes to the test house
• Engineering Design Document AgentA complete, accurate design document that matches the real design
• Requirements Traceability AgentEvery in-scope requirement is linked to delivered work and a passing test
• Standards Compliance Matrix AgentA complete, current compliance matrix for every applicable clause
• Design Review Package AgentComplete, consistent review packages and tracked actions

Connections (MCP servers) 12

A guide in the download. A connection lets your AI work in an app you already use. You add only the ones you use: ask your AI "Which apps can you connect to?" and follow the steps on each connection's page.

• Tech Trend MCP serverYour AI can gather fresh research papers, trending code, and FDA device news, then write you a short newspaper-style briefing.
• Scholar MCP serverYour AI can search academic papers, read them, map citations, and save them into a personal library.
• Research Hub MCP serverLets your AI search for papers, save them to Zotero, and write notes into your Obsidian vault for you.
• NCBI PubMed MCP serverSearch PubMed's millions of research articles and get summaries, authors, and related papers through your AI.
• Patsnap Patent & Literature Search MCP serverLets your AI search global patents and scientific papers in plain language and pull back readable records. No install needed.
• Google Scholar MCP serverLets your AI search Google Scholar and pull ready-made citations for papers you find. No install needed.
• Mendeley MCP serverLets your AI search your Mendeley library, read your papers, and organize your folders for you.
• arXiv MCP serverLets your AI search arXiv for research papers and pull up their details and full text. No install needed.
• Web Researcher MCP serverLets your AI search trusted sites, read full articles, and give you real, clickable sources.
• MATLAB MCP serverLet your AI write and run MATLAB code, make interactive plots, and run long jobs for you.
• Annota MCP serverLet your AI read your Zotero papers, highlight key findings, explain formulas, and save reading notes back to your library.
• Bing Search MCP serverLets your AI search the web, news, and images through Microsoft Bing while you chat.

Your Grok Bot team 12

• Quality Documentation ManagerManages document control, change control, and regulatory documentation compliance for medical device organizations.
• Mdr 745 SpecialistGuides medical device manufacturers through EU MDR 2017/745 compliance, from classification to post-market surveillance.
• Fda Consultant SpecialistProvides FDA regulatory pathway, QSR compliance, HIPAA, and cybersecurity guidance for medical device companies.
• Regulatory Affairs HeadManages regulatory strategy and submissions for HealthTech and MedTech devices.
• Risk Management SpecialistManages ISO 14971 risk management files for medical devices throughout the product lifecycle.
• Quality Manager Qms Iso13485Helps you implement and maintain an ISO 13485 QMS for medical devices.
• Fda Medtech Compliance AuditorAudit medical device software compliance against FDA and ISO standards.
• Clinical ReportsWrites clinical reports with regulatory compliance and validation tools.
• Technical WriterCreates and improves technical documentation for APIs, SDKs, and user guides.
• Documentation ExpertCreates, improves, and maintains project documentation from code and specs.
• PrototypeBuild a throwaway terminal or UI prototype to answer one design question fast.
• Atlassian Requirements to JiraParse requirements documents and create Jira epics and user stories with duplicate detection and approval workflow.