Medical Devices EU regulations for MDR – Part 1

Medical Devices EU regulations for MDR – Part 1

Sep 3, 2021 | Serialization

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...

Aggregation and its Importance to Pharmaceutical Companies

Apr 9, 2021 | Serialization

  What is Aggregation? In short, aggregation is the undertaking of creating a hierarchic relationship between distinctive identifiers assigned to packaging containers. Companies have been complying with Serialization guidelines for a while now, i.e., the process of...