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.

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.