Medical Devices EU regulations for MDR – Part 1

Medical Devices EU regulations for MDR – Part 1

Introduction The EU MDR is a new set of regulations that came into effect on 26th May 2021, following a 4-year transition period after being adopted in May 2017. It aims to improve the safety and performance of the device throughout the lifecycle by tightening up the...
SFDA Dossier requirements

SFDA Dossier requirements

  The SFDA Dossier requirements differ for each application. What is important to note is that the CTD provides a format for an MAA (Marketing Authorization Applcication) Also to be noted is that regional and national requirements may affect the content of a...
The trending supply chain technologies in 2021

The trending supply chain technologies in 2021

The past decade has seen major breakthroughs in technology and though there have been really great strides, the pace of innovation in technology is still on at an ever increasing pace. Here are some present and rapidly advancing supply chain technologies that you...
What is VRS?

What is VRS?

VRS or Verification Router Service is an automated way of verifying saleable returns to improve supply chain efficiency while maintaining the integrity of the supply chain and keeping it free from counterfeit drugs.   What are saleable returns? When products are...