An administrative change of a product requiring prior notification before implementation is an administrative change, the knowledge of which is important for purposes of control and enforcement. Such changes include those listed in the following table, provided that the conditions therein are met:

Name of the biocidal product
1.	Changes of the name of the biocidal product where there is no risk of confusion with the names of other biocidal products.
2.	Addition of a name for the biocidal product where there is no risk of confusion with the names of other biocidal products.
Authorisation holder
3.	Transfer of the authorisation to a new holder established in the United Kingdom.
4.	Change in the name or address of the authorisation holder, which remains in the United Kingdom.
Manufacturer(s) of the active substance(s)
5.	Addition of a manufacturer of the active substance or change in the manufacturer’s identity or in manufacturing location or process, where the technical equivalence between the substances from the two manufacturers, manufacturing locations and processes has been established by the competent authority in accordance with Article 54 of Regulation (EU) No 528/2012, and the manufacturer or importer is listed in accordance with Article 95(2) of Regulation (EU) No 528/2012.
Biocidal product family
6.	Authorisation as a biocidal product family of a number of authorised products falling within the specifications of a frame-formulation established in accordance with Directive 98/8/EC in accordance with the same terms and conditions.

An administrative change of a product which can be notified after implementation is an administrative change, the knowledge of which is not important for purposes of control and enforcement. Such changes include those listed in the following table, provided that the conditions therein are met:

OJ L 353, 31.12.2008, p. 1.
Authorisation holder
1.	Change in other administrative details of the authorisation holder than the name and address.
Formulator(s) of the biocidal product
2.	Change in the name, the administrative details or the formulating location of the biocidal product formulator, where the biocidal product composition and the formulating process remain unchanged.
3.	Deletion of a formulating location or a formulator of the biocidal product
4.	Addition of a formulator of the biocidal product, where the biocidal product composition and the formulating process remain unchanged.
Manufacturer(s) of the active substance(s)
5.	Change in the name or the administrative details of a manufacturer of the active substance, where the manufacturing location and process remain unchanged and the manufacturer remains listed in accordance with Article 95(2) of Regulation (EU) No 528/2012
6.	Deletion of a manufacturer or a manufacturing location of the active substance
Conditions of use
7.	More precise instructions for use, where only wording but not content of instructions are changed.
8.	Removal of a particular claim, such as a specific target organism or a specific use.
9.	Removal of a category of users.
10.	Addition, replacement or modification of a measuring or administration device not relevant for the risk assessment and not regarded as a risk mitigation measure.
Classification and labelling
11.	Change to the classification and labelling, where the change is limited to what is necessary to comply with newly applicable requirements of Regulation (EC) No 1272/2008 of the European Parliament and of the Council.