Understanding the FDA Cybersecurity Go-Team

Understanding the FDA Cybersecurity Go-Team

Understanding the FDA Cybersecurity Go-Team The U.S. Food and Drug Administration (FDA) recently unveiled the Medical Device Safety Action Plan: Protecting Patients, Promoting Public Health, a comprehensive plan with the goal of assessing processes and procedures in...
From On-Screen To Real Life

From On-Screen To Real Life

From On-Screen To Real Life "Chicago Med" Explores FDA Guidelines The US Food and Drug Administration (FDA) recently released a new medical device safety action plan that contains five focus areas that aim to improve the quality of real-world evidence,...
Top Challenges in Strategic Sourcing and How to Combat Them

Top Challenges in Strategic Sourcing and How to Combat Them

Top Challenges in Strategic Sourcing and How to Combat Them A Q&A with Patrick Smith from ProNova The ultimate goal of those involved in sourcing and procurement is to procure components for the best value possible. Individuals with sourcing and procurement all...
Is IoT Technology Making the Internet Irrelevant?

Is IoT Technology Making the Internet Irrelevant?

Is IoT Technology Making the Internet Irrelevant? Medical Device Field Service Perspective As information technology continues to develop and reinvent itself, old technology is declared irrelevant and replaced. The same can be argued for the Internet. We are now at...
How Clinical Education Will Evolve in the Next 5 Years

How Clinical Education Will Evolve in the Next 5 Years

How Clinical Education Will Evolve in the Next 5 Years How Clinical Education Will Evolve in the Next 5 Years Clinical Training and Education is an industry that faces many unique challenges. Educating customers on technical, clinical, and procedural uses of medical...
Preparing For Your Clinical Evaluation Report

Preparing For Your Clinical Evaluation Report

Preparing For Your Clinical Evaluation Report Preparing For Your Clinical Evaluation Report Aligning with MEDDEV 2.7.1 and the MDR The newest revision has defined, clarified and tightened guidance on clinical evidence requirements for unapproved technologies as well...