Greece to register all medical products
This article was originally published in Clinica
The Greek authorities will require registration for all medical devices sold on their territory. The Health Ministry's biomedical division, the Competent Authority since January 1st this year, is preparing legislation which it hopes to introduce in September. At present, registration is only required for medical devices in Class I of the Medical Devices Directive, for custom-made devices and sterilised products.
You may also be interested in...
Recent and upcoming US FDA advisory committee meetings and a summary of topics covered.
The Swiss giant is hoping to get seven more approvals for its blockbuster immunology drug over the next 10 years.