Free Resources For The Medical Device Industry

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From Box-Checking to Breakthroughs: How Regulatory Compliance Fuels Innovation in MedTech

From Spreadsheets to Simplicity: How Magsorbeo Built a Compliant, Scalable QMS with QuickVault

Mastering eSTAR: Step-By-Step Guide to Seamless Submissions

QuickVault Launches New Regulatory Submission Functionality

When Is the Right Time for a MedTech Startup to Implement a Quality Management Solution?

Comprehensive Guidance on QMS setup for MedTech startups

Navigating MedTech eQMS Selection: A Comprehensive Guide to Informed Decision-Making

IQ, OQ, PQ Checklist Bundle

510(k) Documentation Readiness Checklist

User Needs vs. Design Inputs: Cheat Sheet for MedTech Teams

Go-to-Market Content Bundle for MedTech Teams

Mastering eSTAR Submissions eBook

Performance Qualification (PQ) Checklist

Operational Qualification (OQ) Checklist

Installation Qualification (IQ) Checklist

Preventive Maintenance Form

Training Matrix Form

Risk Management Plan Form

Design Plan Template

MedTech QMS Implementation: Understanding the Why, What, When, and How

MedTech Regulatory Submissions Made Easy

QuickTalk Episode 7: MedTech Startup Law: Legal Support for Formation, Fundraising & Exit

QuickTalk Ep6: Understanding reimbursements is an essential skill for a MedTech’s success

Navigating Cybersecurity in MedTech: Key Insights from QuickTalk Episode #5

Harnessing Early Commercialization Strategies for MedTech Success: Insights from QuickTalk Episode #4 with Tom Ross

Leveraging Your Brand & Telling An Exciting Story

QuickTalk Episode #2: Clear Concise Communication

QuickTalk Ep1: Special Guest Carolyn Guthrie discusses the FDA QMSR Changes

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17 Apr 2024

Resource Center

MedTech QMS Implementation: Understanding the Why, What, When, and How

Tackling Your First 510(k): Advice from Top MedTech Consultants

IQ, OQ, PQ Checklist Bundle

510(k) Documentation Readiness Checklist

User Needs vs. Design Inputs: Cheat Sheet for MedTech Teams

How to Determine User Needs for a Medical Device (Without Overthinking It)

Go-to-Market Content Bundle for MedTech Teams

Mastering eSTAR Submissions eBook

Performance Qualification (PQ) Checklist

Tackling Your First 510(k): Advice from Top MedTech Consultants

How to Determine User Needs for a Medical Device (Without Overthinking It)

From Box-Checking to Breakthroughs: How Regulatory Compliance Fuels Innovation in MedTech

From Spreadsheets to Simplicity: How Magsorbeo Built a Compliant, Scalable QMS with QuickVault

Mastering eSTAR: Step-By-Step Guide to Seamless Submissions

QuickVault Launches New Regulatory Submission Functionality

When Is the Right Time for a MedTech Startup to Implement a Quality Management Solution?

Comprehensive Guidance on QMS setup for MedTech startups

Navigating MedTech eQMS Selection: A Comprehensive Guide to Informed Decision-Making

IQ, OQ, PQ Checklist Bundle

510(k) Documentation Readiness Checklist

User Needs vs. Design Inputs: Cheat Sheet for MedTech Teams

Go-to-Market Content Bundle for MedTech Teams

Mastering eSTAR Submissions eBook

Performance Qualification (PQ) Checklist

Operational Qualification (OQ) Checklist

Installation Qualification (IQ) Checklist

Preventive Maintenance Form

Training Matrix Form

Risk Management Plan Form

Design Plan Template

MedTech QMS Implementation: Understanding the Why, What, When, and How

MedTech Regulatory Submissions Made Easy

QuickTalk Episode 7: MedTech Startup Law: Legal Support for Formation, Fundraising & Exit

QuickTalk Ep6: Understanding reimbursements is an essential skill for a MedTech’s success

Navigating Cybersecurity in MedTech: Key Insights from QuickTalk Episode #5

Harnessing Early Commercialization Strategies for MedTech Success: Insights from QuickTalk Episode #4 with Tom Ross

Leveraging Your Brand & Telling An Exciting Story

QuickTalk Episode #2: Clear Concise Communication

QuickTalk Ep1: Special Guest Carolyn Guthrie discusses the FDA QMSR Changes