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

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Outsourcing Clinical Activities in 2024: Choosing A CRO

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

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

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Why is Post-Market Surveillance Important for Medical Devices?

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5 Postmarket Surveillance System Musts for Every EU Manufacturer

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[VIDEO] 7 Ways to Track QMS Effectiveness using Medical Device Post-market Quality Processes (Track Phase)

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Understanding Post-Market Surveillance Requirements for Medical Devices (US & EU Markets)

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

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Navigating Clinical Evaluations and Investigations in MedTech

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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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How to Structure a Clinical Investigation Report (CIR) Summary

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

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

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4 Reasons to Stop Mixing Your Clinical Data Collection Methods

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

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Electronic Data Capture Systems vs. Paper-based data collection

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

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How to use eConsent Efficiently in Medical Device Studies

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Best Practices for eConsent in Medical Device Clinical Investigations

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

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

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Electronic Data Capture for Medical Devices: Then vs. Now

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How to Use Greenlight Guru Clinical's ePRO Module

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

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10 Tips for Selecting the Right EDC Software for Clinical Investigations

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8 Tips Before Calculating Sample Size in Medical Device Clinical Studies

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Everything You Need to Know about Electronic Data Capture (EDC) Systems

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10 Best Practices for eCRF in Medical Device Trials

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Guidance on How to Conduct Clinical Investigations Under EU MDR

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Compliant Adverse Event Reporting in Clinical Studies under the EU MDR

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eCRF Template for Clinical Investigations and PMCF Studies

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

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

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How to Calculate Sample Size for Medical Device Studies

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Setting up a Clinical Investigation under EU MDR

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Alternatives to PMCF Clinical Investigations

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

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

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The Medical Device Practical Guide to PMCF Requirements under EU MDR

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Selecting The Ideal PMCF Activity

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

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Ultimate Guide to Clinical Data Management in MedTech

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

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How to Carry Out PMCF Activities According to EU MDR

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Greenlight Guru Introduces Quality Event Automation to Advance Efficiencies in the Management of Post-Market Quality Events

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