Pristojni organ zadevne države članice s ponavljajočimi inšpekcijskimi pregledi in, če je potrebno, z nenapovedanimi pregledi, ter s prošnjo za testiranje vzorcev, naslovljeno na Uradni kontrolni laboratorij za preskušanje zdravil ali laboratorij, pooblaščen za ta namen, zagotovi, da se pravne zahteve, ki urejajo področje zdravil, izpolnjujejo.
The competent authority of the Member State concerned shall ensure, by means of repeated inspections, and if necessary unannounced inspections, and, where appropriate, by asking an Official Medicines Control Laboratory or a laboratory designated for that purpose to carry out tests on samples, that the legal requirements governing medicinal products are complied with.