EU devices committee aims to make addresses on labels consistent
This article was originally published in SRA
The EU medical device Central Management Committee has issued a decision that aims to ensure uniformity in how manufactures display their address on device labels and instructions for use1,2.
You may also be interested in...
While good clinical practice inspectors in the UK and the US collaborate on matters of common interest, they say that mutual recognition is simply not possible.
Whoever takes over as chair of the Medicines and Healthcare products Regulatory Agency will play a key role in its plans to deliver a program of “ambitious business change.”
The International Council for Harmonisation has replaced its 1993 guideline on reproductive toxicity studies with an updated version.