1 The Responsible Person is responsible for the direct technical supervision of the facilities and in particular ensures that the medicinal products are handled appropriately.
2 They are responsible for the quality of the manufactured medicinal products and ensure that the legal provisions applicable to therapeutic products are observed.
3 They are authorised to issue instructions within their sphere of activity.
4 They and the company management jointly ensure their deputisation by adequately qualified specialists.
5 If the facilities cease operations, or if operations can be expected to cease imminently, the Responsible Person must report this situation to Swissmedic without delay.
6 They may not sit on one of the facilities’ supervisory committees and must decide on the release or rejection of batches independently of the company’s management. Swissmedic may grant a licence to small facilities without such segregation if they cannot implement the segregation because of their size.
7 If the size and nature of the facilities permit this activity to be performed on a part-time basis, responsibilities must be set out in writing and the minimum number of hours during which the person must be present in the facility must be determined.
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This document is not an official publication. Only the publication of the Federal Chancellery is legally binding.
Dies ist keine amtliche Veröffentlichung. Massgebend ist allein die Veröffentlichung durch die Bundeskanzlei.