YOU'LL RECEIVE THE FOLLOWING RESOURCES: |
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✔ Product Development Checklist✔ Risk Management Plan Template✔ 10 Questions to Define User Needs✔ Industry Standards Infographic✔ Design History File Checklist✔ ISO 14971 Risk Management Infographic✔ Cheat Sheet for Preparing your Team for an FDA Inspection✔ 5 Common 510(K) Submission Mistakes✔ Case Study: How Innovere Accelerated Their Path To Market By Implementing Greenlight Guru’s Medical Device eQMS✔ Case Study: How Greenlight Guru Is Laying The Foundation For Success at Amnion Life✔ Case Study: Centese Ditches Paper-based QMS And Achieves FDA 510(k) Clearance✔ Case Study: Photonicare Adopts MDQMS to Accelerate Time to Market |
✔ eBook: 15 Items Med Device Startups Need to Address✔ eBook: A Complete Guide to Bringing a Medical Device to Market✔ eBook: The Ultimate Guide to Design Controls for Medical Device Startups✔ eBook: Defining Design Inputs & Design Outputs✔ eBook: A Step by Step Guide to Determine How your Device Will be Classified✔ eBook: Why Paper-based QMS Are No Longer An Option✔ eBook: Beginner's Guide to Design Verification and Validation✔ eBook: Managing Changes for Medical Devices✔ eBook: 15 Reasons why Medical Device Companies Choose Greenlight Guru✔ eBook: A Step-by-Step Guide to Preparing your 510(K) Submission
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