Biocidal Products Regulations (Northern Ireland) 2001 No. 422

Regulations 10(4) and 12(5) and (7)

SCHEDULE 4 Information to be contained in a dossier submitted in support of an application for the registration of a biocidal product

1.  The name and address of the applicant.

2.  The name and address of the manufacturer of the biocidal product.

3.  The name and address of the manufacturer of the active substance in the biocidal product, and the location of manufacture.

4.  The trade name of the biocidal product.

5.  The name of each substance in the biocidal product, including the name of its active substance, and the amount of each substance, as a percentage of the whole.

6.  The physical and chemical properties of the biocidal product relating to use, storage and transport.

7.  The product-type and field of use of the biocidal product.

8.  The intended category of users.

9.  The intended method of use.

10.  Efficacy data.

11.  Analytical methods.

12.  The classification, packaging and labelling of the biocidal product, including a draft label.

13  Where the biocidal product is a substance or preparation dangerous for supply within the meaning of regulation 2(1) of the 1995 Regulations (1), a safety data sheet for that biocidal product prepared in accordance with regulation 6 of those Regulations.

(1)

S.R. 1995 No. 60, as amended by S.R. 1996 No. 376, S.R. 1997 No. 398, S.R. 1998 No. 459, S.R. 1999 No. 150, S.R. 1999 No. 303 and S.R. 2001 No. 168