LAW ON BIOCIDAL PRODUCTS

authorisation or temporarily permit as well as on the basis of the data referred to in Article 26Paragraph 3 and Article 32 Paragraph 3 of this Law, keep the Register of the BiocidalProducts as a an integral part of the Integrated Chemicals Registry established by the separatelaw regulating chemicals.The Register of the Biocidal Products shall in particular contain: name and address ofthe holder of the Decision on inclusion of the biocidal product into the Temporary List, holderof the authorisation or holder of the temporarily permit as well as the number, date of issuingand period of validity of such acts; name and properties of active substances and othersubstances contained in biocidal product; classification of all hazardous active substances andother hazardous substances contained in biocidal product; trade name of the biocidal product;biocidal product type and authorised uses; formulation of the biocidal product (liquid,granules, powder, solid); tariff heading; maximum residue limit if available; conditions forplacing on the market and use of the biocidal product; as well as safety data sheet.The Agency shall, annually, publish in the “Official Gazette of the Republic of Serbia”following data from the Register of Biocidal Product: name and address of the holder of theDecision on inclusion of the biocidal product into the Temporary List or holder of theauthorisation; trade name of biocidal product; number, date of issuing and period of validity ofsuch acts.VI. RESEARCH AND DEVELOPMENT OF THE BIOCIDAL PRODUCTArticle 35Biocidal product, for which the Decision on inclusion into the Temporary List or theauthorisation was not issued, may be placed on the market only for the purposes of scientificresearch and development or process-orientated research and development.The Agency shall issue the certificate for placing on the market of the biocidal productused for process-orientated research and development.Manufacturer or importer of the biocidal product shall, along with the application forissuing of the certificate referred to in Paragraph 2 of this Article, submit the data on the activesubstance or biocidal product, in particular: identity; data on labelling; data on quantities to beused; name and addresses of those persons who will use it; effects of that active substance orbiocidal product on human or animal health or impact on the environment, if available as wellas the envisaged date of starting and completing of the research.Person carrying out scientific research and development or process-oriented researchand development shall make a report on the biocidal product for which he conducted theexperiment and such report shall contain: data on identity, data on labelling, quantities in use,persons using it as well as data on the effect of the active substance or biocidal product onhuman and animals health and impact on the environment, if available.Persons carrying out scientific research and development or process-orientatedresearch and development shall submit the report referred to in Paragraph 4 of this Article tothe Agency upon request.16