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Authority News |
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15 June 2010 New Practice for Authorisation of Qualified Persons on Section 39 Authorisations As of 27 May 2010, the Danish Medicines Agency permits Danish companies authorised
pursuant to section 39 of the Danish Medicines Act to manufacture and import medicinal products and
intermediate products to have more than one qualified person authorised and named on the section 39
authorisation. |
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