Turning Complex Medical Data Into Engaging Reader-Friendly Stories
Turning Complex Medical Data into Engaging, Reader-Friendly Stories How to Transform Evidence into Clear, [...]
Self-Certification for CE Mark – An Overview
The gradual implementation of the European Medical Device Regulation (MDR, 2017/745) changed the game [...]
The UK MDR and The EU MDR: What Are The Differences?
UK MDR is the primary standard that mandates requirements for anyone selling medical products [...]
Post-market Clinical Follow-up (PMCF): What you Need and How to Get It
One of the new aspects introduced in the European Medical Device Regulation 2017/745 (MDR) [...]
Before You Hire a Clinical Evaluation Consultant: Read This
Thinking of Hiring a Clinical Evaluation Consultant? So it's finally time to either start [...]
The DIY Clinical Evaluation Report – Do You Really Need A CER Writer?
So you’ve taken a look at EU MDR transitions for some of your devices and [...]
ISO Standards for Medical Devices: What they are and When you Need Them
The whole point of medical devices is to improve patient safety and patient quality [...]
Systematic Literature Review Course – Onboarding: Welcome!
Welcome to the Systematic Literature Review Course! We’re thrilled to have you on board. [...]
Lesson 1 – Systematic Literature Review Course: Search Protocol Key Sections
Missed last week? Read our Past Lesson: Onboarding. Be sure to check it out if you haven’t [...]
Lesson 2 – Systematic Literature Review Course: Selecting Your S&P Criteria and Clinical Claims
Missed last week? Read our Past Lesson: Search Protocol Key Sections. Be sure to check it [...]