Ordinance
on the Placing on the Market and Handling of Biocidal Products
(Ordinance on Biocidal Products, OBP)


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Art. 13e Record-keeping requirements for research and development

1 Any­one who, for pur­poses of re­search and de­vel­op­ment, handles un­au­thor­ised biocid­al products or non-ap­proved act­ive sub­stances for use in biocid­al products must keep re­cords de­tail­ing the fol­low­ing:

a.
iden­tity of the biocid­al products or act­ive sub­stances;
b.
la­belling data;
c.
quant­it­ies sup­plied;
d.
name and ad­dress of the per­son re­ceiv­ing the biocid­al products or act­ive sub­stances;
e.
all avail­able data con­cern­ing pos­sible ef­fects on hu­mans, an­im­als or the en­vir­on­ment.

2 The re­cords shall be made avail­able to the No­ti­fic­a­tion Au­thor­ity on re­quest.

3 The No­ti­fic­a­tion Au­thor­ity may, if ne­ces­sary, re­quest fur­ther in­form­a­tion.

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