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Blog

The 5 most common clinical data pitfalls in 2025 (and how to avoid them)

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Facing uncertainty: how medical device companies are navigating the current economic conditions

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Introducing Document Comparison: Boost Audit Readiness, Accelerate Training, and Streamline Approvals

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Clinical Trials in 2025: The Outlook for Medical Device Companies

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What’s New in Greenlight Guru Clinical 2025.1: Smarter Show Rules and Easier File Vault Access

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The Biggest Quality Challenges for Medical Device Companies in 2025

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5 Common Regulatory Pitfalls in the Medical Device Industry (and How to Avoid Them)

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2025 Medical Device Industry Report: Quality Challenges, Regulatory Complexity, and Economic Uncertainty

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Notification of a Manufacturing Discontinuance or Interruption: Does the FDA’s Guidance Apply to You?

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3 Insights on MedTech Product Development from an Ex-FDA Investigator

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How to Create a Quality Manual per ISO 13485 (Plus Free Template)

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How to Build Your Own GSPR Checklist (Plus Free Template)

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Improving Clinical Data Collection with Effective eCRF Completion Guidelines

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How to Use an FMEA Template as Part of Your Medical Device Risk Management

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Developing a PMCF Plan: Your Blueprint for Regulatory Compliance

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3 Key Steps for Supplier Risk Assessment in MedTech

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Navigating FDA Guidance on Electronic Systems, Records, and Signatures in Clinical Investigations: A Comprehensive Overview for Medical Device Companies

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Most Popular Medical Device Content in 2024

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Top Medical Device Conferences To Attend in 2025

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QMS Implementation: The Key Steps and Tips for Implementing an eQMS

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Creative Clinical Recruitment: 4 Steps to Overcome Barriers to Participation

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Medical Device Compliance: Regulations, Standards, and Solutions

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Enhanced Consenting Options for Clinical Studies

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The FDA Medical Device Approval Process: Pathways, Timelines, and Tips

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FDA's Predetermined Change Control Plan: What's in the New Draft Guidance

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Quality Management Consulting: How and When to Seek Help

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Decentralized Clinical Trials: Are Remote Elements Right for Your Next Study?

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Building an Effective CAPA Program: Key Steps and Common Challenges

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Why Your Company Needs a QMS Software or eQMS

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Market Access vs Adoption: Why Your Class II Device Needs Clinical Evidence

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Real-World Data and Real-World Evidence: When and How to Use Them

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Ultimate Guide to In Vitro Diagnostic (IVD) Devices

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A Free CAPA Template for the Medical Device Industry

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7 Steps to Respond to FDA 483 Inspection Observations (Response Template Included)

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Cybersecurity for Medical Devices: Best Practices from Regulatory Standards

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Strategies for Successful PMA Submissions: A Guide for Clinical Teams

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Top 100 Medical Device Acronyms & Terminology You Need to Know

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QMSR Explained: What FDA QSR & ISO 13485 Harmonization Means for Medical Device Companies

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How to Set Up Clinical Studies to Comply with US FDA Regulations

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5 Elements that Must Connect to Your Design Controls for an Audit-Proof QMS

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Post-Market Surveillance for Medical Devices & IVDs: Requirements & Proactive Data Collection

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Data Management and Reporting in FDA-Regulated Clinical Trials

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Biocompatibility Testing for Medical Devices 101

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Direct to Consumer - The Future of Healthcare

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How 4 Pre-Market MedTech Companies are Leveraging Greenlight Guru Quality

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Quality Management Audit or Assessment? The Differences Explained

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A Guide to Bridging User Needs Into Design Requirements

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ISO 13485 and FDA QSR: A Step-by-Step Guide to Complying with Medical Device QMS Requirements

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MDR and IVDR: Challenges and Opportunities of the New Regulations

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Paper Systems Are the Riskiest Way to Manage Medical Device Projects

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6 Medical Device Product Development Steps To Fast-Track Your Path To Market

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LDT Enforcement Discretion Phaseout: What You Need to Do in the First Year

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2024 Greenlight Guru True Quality Roadshow: Copenhagen Recap

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Why FMEA is Not ISO 14971 Risk Management

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How to Define Your Design Inputs and Design Outputs

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How to Carry Out PMCF Activities According to EU MDR

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FDA Issues LDT Final Rule to Regulate Laboratory Developed Tests as IVD Devices

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QMSR & the End of DMR, DHR, DHF: How FDA’s New Rule Impacts Record-Keeping

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3 Types of QMS Audits (Plus 3 Tips to Prepare for Them)

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FDA’s PMA Supplements and Amendments: When and How to Use Each

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Design History File (DHF) vs. Device Master Record (DMR) vs. Device History Record (DHR): What's the Difference?

Blog

IQ, OQ, PQ: A Quick Guide to Process Validation (Plus Free Resources)

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MDCG 2024-5: Guidance on the Investigator’s Brochure Explained

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Beginner's Guide to Design Verification & Design Validation for Medical Devices

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Ultimate Guide to Device Class Requirements under EU MDR

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Entering the Australia & New Zealand Markets: What Medical Device Manufacturers Need to Know

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QMS Principles for Software As a Medical Device (SaMD) Manufacturers

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Here Are the 4 Types of FDA Inspections You Need to Understand

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ISO 14971 Risk Management for Medical Devices: The Definitive Guide

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How are Medical Devices Classified under EU MDR?

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MDCG 2024-3: What the Latest Guidance on Clinical Investigation Plans (CIP) Tells Us

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The Risk Management + Design Controls Connection: What Device Makers Need to Know

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Definitive Guide to Change Management & Change Control for Medical Devices

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Top 50 Medical Device Product Design and Development Companies

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Ultimate Guide to Clinical Data Management in MedTech

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FDA 510(k) Submission Process: A Step-By-Step Guide On How To Prepare Yours

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What is a Class III Medical Device in the US?

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Improving Study Management in MedTech with Greenlight Guru Clinical’s Custom Collaborator Roles

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Greenlight Guru Shines in G2 Spring 2024 Report, Dominating in Medical QMS and EDC Categories

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Meeting Timelines and Managing Budgets - Best Practices for MedTech Clinical Investigations

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FDA Medical Device Classifications - How To Determine Your Device Class

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ISO 13485: Ultimate Guide to Medical Devices QMS

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Step-by-Step Guide to FDA PMA Submissions for Class III Medical Devices

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How to Take Control of Training Management and Stay Compliant with ISO 13485:2016 and Part 820.25

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Ready to Submit Your FDA 510(k)? But Wait, There's No Human Factors!

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The Ultimate Guide To Design Controls For Medical Device Companies

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Quality Management Plan - How to Create Yours (Tips & Best Practices)

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How to Structure your Medical Device Technical File

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Adopting AI in Quality Management: Practical Solutions for the MedTech Industry

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Outsourcing Clinical Activities in 2024: Choosing A CRO

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Quality Assurance vs. Quality Control in the Medical Device Industry

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ALM and Design Controls: Do SaMD and SiMD Manufacturers Need Both?

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How MHRA is Regulating Medical Devices in the UK after Brexit

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Investigator Initiated Studies — 3 Common Problems and How to Fix Them

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5 Habits of Highly Effective MedTech Companies

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How to Use the Turtle Diagram for Better Internal Audits

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Greenlight Guru Announces the 2024 True Quality Roadshow

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Clinical Data Collection - 7 Key Pitfalls To Avoid In MedTech

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FDA Publishes Final Rule on QMSR

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Introducing Risk Reviews for Efficient, Compliant Risk Management

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Calculating Nonconformance Costs in the MedTech Industry

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Selecting a Notified Body: How to Work with Your New Device Authority

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Greenlight Guru Finishes 2023 with Strong Momentum in Q4

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IVDR: How to Meet the Quality Management System Requirements of a Device

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Navigating Clinical Evaluations and Investigations in MedTech

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How PLM and QMS Solutions Work Together in MedTech

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Guide to Managing Your Medical Device on the Market and Scaling Manufacturing

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Greenlight Guru’s MedTech Suite Named a Leader in G2 Winter 2024 Grid Report

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Customers Rank Greenlight Guru Quality as Medical QMS Leader in G2 Winter 2024 Report

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Greenlight Guru Clinical: Leader in the EDC Category in G2 Winter 2024 Grid Report

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Most Popular Medical Device Content in 2023

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Moving MedTech Forward: Greenlight Guru’s 2023 in Review

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Top 40+ Medical Device Contract Research Organizations (CROs)

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Electronic Data Capture (EDC) Buyer’s Guide: Making the Business Case for a New EDC System

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AI, Automation, and Risk in MedTech

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A Better Way to Develop a Medical Device with Digital and Physical Elements (Part 1 of 2)

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A Better Way to Develop A Medical Device with Digital and Physical Elements (Part 2 of 2)

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The Ugly Truth About Managing Design Controls on Spreadsheets

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Enterprise Quality Management System Software: What You Need To Know

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Ultimate Guide to Supplier Management for Medical Device Companies

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Greenlight Guru Releases The AI in MedTech Trend Report 2023

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The AI in MedTech Trend Report 2023 Is Here

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Mastering the CAPA Process: A Comprehensive Step-by-Step Guide with Free Infographic

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Benefits of Switching from MasterControl to Greenlight Guru

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Reducing Medical Device Risk with Usability Testing: The Why, the How, and the Who

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Ultimate Guide to Software as a Medical Device (SaMD)

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Top 7 QMS Tools for MedTech (Plus 4 Bonus Resources)

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Ultimate Internal Audit Checklist: FDA QSR & ISO 13485 Audit Checklist

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Greenlight Guru Expands Market Leadership with Strong Momentum in Q3 2023

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IVDR for In Vitro Diagnostic Medical Device Companies - Ultimate Guide

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5 Foundational Steps of a CAPA Quality Process

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Ultimate Guide to Corrective and Preventive Action (CAPA) for Medical Devices

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EU MDR - 9 Top Questions Answered (European MDR)

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FDA Proposes New Rule to Regulate LDTs as IVDs: Here’s What’s at Stake

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23 Must-haves for your Product Requirements Document (Free Checklist + Guide)

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MHRA Guidance Document on Clinical Investigations in UK

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Guide to Understanding AI Applications that Drive Business Value in MedTech

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Greenlight Guru Celebrates 10 Years by Introducing its Multi-Product MedTech Suite

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Introducing The Greenlight Guru MedTech Suite: A Comprehensive Set Of Industry-Specific Solutions

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Ultimate Guide to ISO 14155:2020 for Medical Devices

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How To Approach Supplier Corrective Action Requests (SCAR)

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5 Tips for Medical Device Registration across Global Markets

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Engineering Change Order: Its Role in the Change Management Process

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Greenlight Guru Yet Again Ranked as a Leader in QMS and Medical QMS Categories in G2 Fall 2023 Grid Reports

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How to Structure a Clinical Investigation Report (CIR) Summary

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Creating a Supplier Scorecard for Medical Device Supplier Management

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What is a Predetermined Change Control Plan (PCCP) and Who Needs One?

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3 Tips for Adding Flexibility to Your MedTech Manufacturing Supply Chain

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What is the FDA Medical Device Registration Process?

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Machine Learning, AI and Risk Management: TIR34971 Explained

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How to Comply with HIPAA and EU GDPR in Medical Device Studies

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Greenlight Guru Invests in State-of-the-Art Arena and Training Facility That Aims to Help Youth Basketball Players On and Off the Court

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Conducting Quality Investigations in Medical Device Manufacturing

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Omnibus Act Impact on Medical Device Cybersecurity

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Boost Efficiency and Decision-Making with Enhanced Clinical Data Reporting

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Greenlight Guru Continues Strong Growth in Q2 2023 Powered by Product Innovation

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How to Improve Detecting, Correcting, and Preventing Nonconformances

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Ultimate List of ISO Standards for Medical Devices

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eQMS Buyer’s Guide: Making the Business Case for a New QMS Solution

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Identifying and Evaluating Medical Device Importers

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Writing a Clinical Investigation Plan (CIP): The Essential Guide

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15 Questions to Ask QMS Software Vendors in the Medical Device Industry

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How to Develop a Risk-Based Approach to Supplier Management

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Customers Rank Greenlight Guru Leader in QMS and Medical QMS Software in G2 Grid Reports for Summer 2023

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Alternatives to PMCF Clinical Investigations

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15 Reasons Why Medical Device Companies Choose Greenlight Guru

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How to Manage Complex Downstream Design Changes to Your Medical Device

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Purpose-Built QMS vs General-Purpose QMS: What You Can Expect From Each

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Greenlight Guru Publishes Independent Study Showing the ROI of eQMS Solutions on MedTech Companies

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How to Plan and Budget for MedTech Clinical Activities

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CSV vs. CSA: Exploring FDA’s New Software Validation Approach

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Making the Business Case for an eQMS Solution for Your Company

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Greenlight Guru Modernizes Validation Approach to Streamline Software Implementation and Adoption for Medical Device Companies

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Managing Major Changes to Medical Device Packaging

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5 Tips for Designing a Medical Device Study Under FDA Requirements

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What is a Modern QMS?

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4 Tips for Managing Your MedTech Portfolio

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How To Use FDA’s Guidance on Post-Approval Studies During Premarket Approval

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2023 Greenlight Guru True Quality Roadshow: San Jose Recap

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How To Vet Medical Device Distributors in Multiple Markets

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What is the Best Way to Structure a Risk Management File?

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7 Tips for FDA 21 CFR Part 11 Compliance

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Understanding ISO 14971 Medical Device Risk Management

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eIFU Requirements: Everything You Need to Know About Electronic Instructions for Use

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5 Dos and Don'ts when Choosing a QMS Solution for Your Medical Device Company

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Introducing Risk Solutions: A New Era in Risk Management for MedTech

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Greenlight Guru Launches AI-Powered Solutions to Enable Better Risk Management for the MedTech Industry

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How to use the Greenlight Guru Clinical AE/SAE reporting module

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Planning Your Medical Device Global Market Regulatory Strategy

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Why Clinical Data Is Essential to Value-Based Healthcare

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3 Things to Love about Internal Audits

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HTEC Group Partners with Greenlight Guru to Accelerate Time-to-Market for Medical Device Companies

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4 Advantages of an eQMS Over a Paper-Based QMS

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How to Use Clinical Data in Medical Device Submissions in the EU & US

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Greenlight Guru Builds Strong Momentum in Q1 2023 as Medical Device Companies Move to Modern Digital Solutions

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4 Reasons to Stop Mixing Your Clinical Data Collection Methods

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How To Avoid a Failed QMS Implementation

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5 Steps for Getting your CE Marking with EU MDR Requirements

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2023 Greenlight Guru True Quality Roadshow: Houston Recap

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Post-Market Clinical Follow-up Under EU MDR: Guide to PMCF Activities

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Can dFMEA and ISO 14971 Co-Exist in Medical Device Risk Management?

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“A Perfect eQMS”: Customers Rank Greenlight Guru #1 QMS in G2 Spring 2023 QMS Grid Report

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ePRO vs Paper: The Debate Over Patient Reported Outcomes Is Over

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From Closed to Connected: Share Data & Unlock Efficiencies with Greenlight Guru’s Export API

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Greenlight Guru Introduces Export API for a Connected Quality Management System

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5 Tips for Running Effective Internal Quality Audits

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eBOM vs mBOM: What’s the Difference?

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Medical Device Adverse Event Reporting Regulations: EU vs. US

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Electronic Data Capture Systems vs. Paper-based Data Collection

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How to Handle Medical Device Adverse Events

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Explaining IVDR Classification for In Vitro Medical Devices

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Create Your GTM Strategy: The Complete Guide to Bringing a Medical Device to Market

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Making the BOM & Design Controls Connection

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Best QMS Software: Ultimate Guide to Comparing Quality Management System Solutions

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Clinical Data Management System (CDMS) for Medical Device Clinical Trials

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Everything You Need to Know About Electronic Data Capture (EDC) for Clinical Trials

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Top 30 MDCG Guidance Documents for Medical Device Companies

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Top 40 IMDRF Technical Documents for Medical Devices

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Good Clinical Practice (GCP) Compliance in Clinical Data Collection

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Comprehensive 21 CFR Part 11 Guide: Requirements and Downloadable Resources

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Research shows eCRFs faster, more reliable than paper CRFs

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How to Define User Needs During Design Controls

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Greenlight Guru Introduces Newly Expanded Global Partner Program

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Does My Device Labeling Comply with 21 CFR 801?

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Utility Patent vs Design Patent: Choosing the Right One for Your Device

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How to Switch from Paper to EDC Systems in Your Next Clinical Study

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Ultimate Guide to Postmarket Surveillance of Medical Devices

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How to Write a Nonconformance Report in 7 Steps

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How to Choose an Electronic Data Capture System to Comply with EU MDR

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Switching to an Electronic Device History Record (eDHR): What Medical Device Companies Should Know

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What is a Class 1 Medical Device?

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FDA Human Factors Guidance Draft: What Medical Device Manufacturers Need to Know

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3 Factors that Impact Application of Decentralized Clinical Investigations for Medical Devices

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Top 100 Medical Device Companies (Free Chart Included)

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How Electronic Data Capture is Transforming the MedTech Industry

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5 Processes You Need to Invest In to Bring a Device to Market

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21 CFR Part 820: Ultimate Guide to FDA's Quality System Regulation (QSR) for Medical Devices

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What is a Document Control System for Medical Devices?

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The Pitfalls of Using Paper and Excel for Clinical Data

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How to use eConsent Efficiently in Medical Device Studies

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Tips for Ensuring Your Clinical Data Complies with FDA's 21 CFR Part 11

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Applying ISO 10993-1 to Medical Device Submission to FDA

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What is an FDA Class 2 Medical Device in the US?

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Top Risk Management Tools in the Medical Device Industry

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Process Verification vs Process Validation: What’s the Difference?

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Best Practices for eConsent in Medical Device Clinical Investigations

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FDA Form 483 Observations and FDA Warning Letters - What’s the Difference?

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What is 21 CFR 812 - Investigational Device Exemption?

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Creating a Periodic Safety Update Report (PSUR) that Complies with MDR & IVDR

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Greenlight Guru Announces 2023 True Quality Roadshow

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Greenlight Guru Releases 2023 MedTech Industry Benchmark Report

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Computer Systems Validation: How To Avoid FDA Warning Letters C.F.R. 820.70(i)

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How to Collect PMCF Data for Lower-Class Medical Devices and WETs

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The Essential Guide to eCRF (Electronic Case Report Form) for Medical Devices

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The Medical Device Development Process: A Deep Dive into the 5 Phases

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How to Plan a Clinical Data Management Setup for EDC Systems

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Greenlight Guru Announces Partnership with Comply Guru

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Understanding FDA Cleared vs Approved vs Granted for Medical Devices

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Explaining the Role of PRRC under MDR & IVDR: Your Questions Answered

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9 Steps to Creating a CAPA Audit Checklist

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The 3 C’s of the EU MDR: Changes, Challenges and Contributions

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GUDID 101: Everything You Need to Know About FDA’s Global Unique Device Identification Database

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How to Manage the Different CAPA Phases

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What is an ISO Audit?

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Tips for Structuring Your Internal Audit Program (and Mistakes to Avoid)

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Medical Device Clinical Trials: Regulatory Pathways & Study Types Explained

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5 Steps For Effective Trial Design and Improved Compliance

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How to Verify and Validate SaMD in Different Stages

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Most Popular Medical Device Content in 2022

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Optimizing Generation of Clinical Evidence for Medical Devices

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Randomization in Medical Device Clinical Trials: Everything You Need to Know

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A Year of Scale, Support, and Celebration

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Design Controls Need to Start With User Needs

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The Importance of Management Reviews for CAPAs

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CAPA Best Practices: 4 Tips for Building an Excellent CAPA Process

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How Technology Can Support Clinical Trial Continuity & Data Integrity

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Greenlight Guru Hits the 1,000 Customer Milestone

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A Letter From the CEO: Celebrating 1,000 Medical Device Customers

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How to Use Greenlight Guru Clinical's ePRO Module

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Electronic Data Capture for Medical Devices: Then vs. Now

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Greenlight Guru Appoints Dan Thompson as Chief Sales Officer and Jeff Perkins as Chief Marketing Officer

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How to Switch to eQMS Software When You're Just Using Paper

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How ePRO Can Help Comply with EU MDR Post-Market Surveillance

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The Difference Between Intended Use and Indications of Use (And Why These Statements Are So Important)

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Nonconformance (NC) and CAPA: When Should You Use Each Process?

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Tracking Serious Adverse Events for Medical Devices (to Ensure GCP Compliance)

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What Device Makers Need To Know About Design Verification and Validation

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Understanding Root Cause Analysis in the CAPA Process

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How Does the EU GDPR Impact Medical Device Clinical Trials?

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How to Integrate Complaint Handling and Risk Management

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8 Tips Before Calculating Sample Size in Medical Device Clinical Studies

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The Difference Between Managing Product & Services Suppliers in MedTech

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MDCG Guidance Documents Overview on Clinical Investigations and Evaluations

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Why Investigator Initiated Studies Alone Are Not the Solution for PMCF Under EU MDR

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Approved Supplier List: How To Add Suppliers to Your ASL in 7 Steps

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3 Common Misconceptions About Medical Device Labeling

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Medical Device QMS + Guru MedTech Experts: A Winning Combo for Global Market Success

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10 Best Practices for eCRF in Medical Device Trials

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15 Steps to Getting Approval for IEC 60601-1 (Staging)

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How to Integrate UDI into a Quality System for Your Medical Device

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Should ISO 15189 Certification Matter to Medical Device Companies?

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Basic UDI-DI: What is it and How to Assign it for Your Medical Device

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Guidance on How to Conduct Clinical Investigations Under EU MDR

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What You Need to Know About Risk Management and Using Post-Market Data

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MDCG 2020-5 Explained: How To Demonstrate Equivalency in the EU

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Computer Software Assurance for Medical Devices: What Does FDA’s Draft Guidance Mean for You?

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Get Compliant Clinical Data with Investigator-Initiated Studies

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Preparing for EUDAMED - Europe’s Medical Device Database

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The Medical Device Practical Guide to PMCF Requirements under EU MDR

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What is a Quality Culture? (and 7 Tips for Creating One)

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3 Tips For Incorporating Risk Management During Medical Device Product Development

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10 Tips for Selecting the Right EDC Software for Clinical Investigations

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Four Years, For You

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15 Steps to Getting Approval for IEC 60601-1

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IEC 82304 vs IEC 62304: Software Standards for SaMD Explained

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Compliant Adverse Event Reporting in Clinical Studies under the EU MDR

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What You Need to Know About Medical Device Software Validation

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MEDDEV 2.7/1 Rev. 4 & MDCG Guidance: Carrying Out Clinical Evaluation Under EU MDR

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eCRF Template for Clinical Investigations and PMCF Studies

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AAMI TIR45: Closing the Gap Between Agile Software Development & Medical Device Regulations

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MDCG 2020-6 Explained: Sufficient Clinical Evidence for Legacy Medical Devices in the EU

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Failure Mode Effects Analysis: What Is It & When Should You Use It?

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The Practical Guide to Post-Market Clinical Follow-up EU MDR Compliance

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Explaining MDCG 2019-11: Software Qualification & Classification for MDR & IVDR

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Bill of Materials (BOM) for Medical Devices: Everything You Need To Know

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How to Design a Successful Post-Market Clinical Follow-Up (PMCF) Survey

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Understanding FDA’s Special 510(k) Program

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How to Communicate Your Regulatory Strategy to Medical Device Investors

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How to Design an Electronic Case Report Form (eCRF) for Medical Device Studies

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How the Design Control Process Applies to a 510(k) Premarket Notification

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How to Use Queries for Monitoring Medical Device Studies in Greenlight Guru Clinical

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Ultimate Guide to UDI for Medical Devices

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Why Class 1 Medical Device Companies Need Design Controls (even if it’s not required)

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How to Calculate Sample Size for Medical Device Studies

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What are the Risk Management Documentation Requirements of ISO 14971?

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3 ISO Compliance Guidelines Every Medical Device Manufacturer Should Follow

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Why is Post-Market Surveillance Important for Medical Devices?

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Why Training Compliance Matters for Pre-Market MedTech Companies

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3 Common Problems with Design Controls (and the Solutions)

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Downstream Effects of Inadequate Complaint Handling

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What are the Distributor Requirements under EU MDR and IVDR?

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Greenlight Guru Further Extends Commitment to Quality for Customers with Earning Both ISO 9001 and ISO 27001 Certifications

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Selecting The Ideal PMCF Activity

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3 Tips for Managing Your Medical Device Design History File

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5 Signs Your MedTech Startup is Ready for the Next Round of Funding

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Understanding The Relationship Between Usability and Labeling of Your Medical Device

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How To Apply a Risk-Based Approach to Biological Evaluation

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4 Letter to File Mistakes That Could Cost You

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Striving for Excellence: G2 Ranks Greenlight Guru #1 in Best Support, Best Usability, and Best Results for QMS

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Understanding Change Management and Change Control in the Medical Device Industry

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Medical Device Companies - Top 100 in 2020 (Free Chart) (Clone)

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3 Stages of Project Management in the Medical Device Industry & How to Navigate Each

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Greenlight Guru Unveils the World's First MedTech Lifecycle Excellence Platform to Enable Success Across The Entire Product Lifecycle

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MedTech Lifecycle Excellence: Out of the Dark and into the Age of Enlightened Quality

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Recap of True Quality 2022

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What Role Should Quality Play in Bringing a Medical Device to Market?

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Who are the Economic Operators & What Does EU MDR Require of Them?

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Applying for International Patents as a Medical Device Company

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Greenlight Guru Acquires Electronic Data Capture Solution SMART-TRIAL

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5 Strategies to Limit Project Timeline and Cost for your Medical Device

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Setting up a Clinical Investigation under EU MDR

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Greenlight Guru Acquires AI/ML Consultancy Vertex Intelligence

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Greenlight Guru Academy Advance: The Future of MedTech Learning is Continuous

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How to Build a Medical Device Business Case in 5 Easy Steps

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FDA De Novo Pathway: Process Explained for Medical Device Companies

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Greenlight Guru Earns 2022 TrustRadius Top Rated Software Award

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8 Questions That Define Your Medical Device User Needs

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