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Showing 1191–1200 of 29699 articles for “Art. Cass. com. 13-9-2011 n° 10-19.907”
A reference medicinal product may belong to both a generic group and a hybrid group as defined respectively in b and d of 5° of Article L. 5121-1.
The authorisation holder has an organisation that ensures that each patient receives treatment that complies with the recommendations or guidelines for good clinical practice defined by the National C…
For the post-operative care of the patients they treat, holders of the authorisation for thoracic oncology surgery with A2 mention mentioned in I of Article R. 6123-87-1, holders of the authorisation…
Each year, the chairman presents his action programme to the grouping medical commission, taking into account actions already implemented. He presents a report on the implementation of the shared medi…
Authorisation may only be granted if the holder has access, on site or by agreement, to medical biology tests and labile blood products within a timeframe that is compatible with the safety of treatme…
The holder of the authorisation ensures that patients are diagnosed and treated on a permanent basis, in liaison with the emergency medicine structures mentioned in article R. 6123-1, including via te…
Authorisation for interventional activity under medical imaging in neuroradiology, category A, may only be granted if the holder has access to a neurosurgery unit, where applicable by agreement. Autho…
Authorisation may only be granted if the holder can provide cerebral and vascular exploration by scanner and MRI, on site, twenty-four hours a day, seven days a week.The holder of the medical imaging…
I.- The processing mentioned in article R. 1461-11 concerns data from the national health data system with a maximum historical depth of :1° 19 years, in addition to the current year, for the Agence n…
In communes of 3,500 inhabitants or more, documents relating to the operation of delegated public services, which must be submitted to the commune pursuant to public service delegation agreements, wit…
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