Description
In a landscape of ever increasing and ever evolving regulatory requirements, developing compliant medical devices packaging and labelling is often challenging. Furthermore, the introduction of unique device identification (UDI) by the FDA and in Europe has added complexity to the already multifaceted medical device labelling strategies. In light of this, Global Medical Device Packaging and Labelling Compliance 2011 will provide the very latest practical insights to enable you to achieve compliant, cost effective and UDI traceable medical device packaging and labelling.
