Ordinance
on Licensing in the Medicinal Products Sector
(Medicinal Products Licensing Ordinance, MPLO)

English is not an official language of the Swiss Confederation. This translation is provided for information purposes only and has no legal force.

of 14 November 2018 (Status as of 1 January 2020)


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Art. 16 Mandatory documentation

Li­cence hold­ers must keep the fol­low­ing doc­u­ments in par­tic­u­lar in or­der to en­sure trace­ab­il­ity:

a.
the name of the medi­cin­al product;
b.
the trans­ac­tion date;
c.
the quant­ity;
d.
the batch num­ber;
e.
the ex­piry date;
f.
the name and ad­dress of the sup­pli­er and the cus­tom­er.
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