Systematic Literature Review Course
Welcome to the Systematic Literature Review Course!
Effectively Handling Corrective and Preventive Actions (CAPA) Process with EU MDR
The EU MDR emphasizes field safety corrective actions to correct non-conformances of the distributed product, but since these principles are [...]
Breaking Down EU MDR Implementation for Class 1 Medical Devices
Breaking Down EU MDR Implementation for Class 1 Medical Devices Following the one-year delay in the MDR Date of Application, [...]
Post Market Surveillance EU MDR – CiteMed
Post-market surveillance (PMS) under the EU MDR (2017/745) is a systematic and proactive process through which medical device manufacturers [...]
Performing Effective Literature Search – For EU MDR and Other Regions
For any medical device, there must be sufficient clinical evidence to corroborate compliance with relevant essential requirements for safety [...]
Systematic Literature Review Course – Onboarding: Welcome!
Welcome to the Systematic Literature Review Course! We’re thrilled to have you on board. Especially in this industry, time [...]
Choosing the Best Systematic Literature Review Tools
We have performed 100s of literature reviews over the last few years across medical device and pharma, and here’s [...]
Common Notified Body Feedback on Literature Review (And How to Address Them)
Who This Was Written For? To celebrate the latest release of our systematic literature review tool, the CiteMed team [...]
The Vital Role of Systematic Literature Review
Introduction to Systematic Literature Reviews Systematic literature reviews stand as a cornerstone in the world of scientific research. Imagine [...]
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 already!” Identifying [...]