Search Legislation

Directive 98/8/EC of the European Parliament and of the Council (repealed)Show full title

Directive 98/8/EC of the European Parliament and of the Council of 16 February 1998 concerning the placing of biocidal products on the market (repealed)

 Help about what version

What Version

 Help about advanced features

Advanced Features

 Help about opening options

Opening OptionsExpand opening options

 Help about UK-EU Regulation

Legislation originating from the EU

When the UK left the EU, legislation.gov.uk published EU legislation that had been published by the EU up to IP completion day (31 December 2020 11.00 p.m.). On legislation.gov.uk, these items of legislation are kept up-to-date with any amendments made by the UK since then.

Changes over time for: Division V.

 Help about opening options

Version Superseded: 01/09/2013

Status:

EU Directives are published on this site to aid cross referencing from UK legislation. Since IP completion day (31 December 2020 11.00 p.m.) no amendments have been applied to this version.

[F1V. EFFECTS ON HUMAN HEALTH U.K.

TIER I U.K.
5.1. Basic information U.K.
5.1.1. Medical data U.K.
5.1.2. Medical surveillance on manufacturing plant personnel U.K.
5.1.3. Sensitisation/allergenicity observations U.K.
5.1.4. Direct observation, e.g. clinical cases U.K.
5.2. Basic studies U.K.
5.2.1. Sensitisation U.K.
5.2.2. Acute toxicity, pathogenicity, and infectiveness U.K.
5.2.2.1. Acute oral toxicity, pathogenicity and infectiveness U.K.
5.2.2.2. Acute inhalation toxicity, pathogenicity and infectiveness U.K.
5.2.2.3. Intraperitoneal/subcutaneous single dose U.K.
5.2.3. In vitro genotoxicity testing U.K.
5.2.4. Cell culture study U.K.
5.2.5. Information on short-term toxicity and pathogenicity U.K.
5.2.5.1. Health effects after repeated inhalatory exposure U.K.
5.2.6. Proposed treatment: first aid measures, medical treatment U.K.
5.2.7. Any pathogenicity and infectiveness to humans and other mammals under conditions of immunosuppression U.K.
END OF TIER I U.K.
TIER II U.K.
5.3. Specific toxicity, pathogenicity and infectiveness studies U.K.
5.4. Genotoxicity — In vivo studies in somatic cells U.K.
5.5. Genotoxicity — In vivo studies in germ cells U.K.
END OF TIER II U.K.
5.6. Summary of mammalian toxicity, pathogenicity and infectiveness and overall evaluation] U.K.

Back to top

Options/Help

You have chosen to open the Whole Directive

The Whole Directive you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.

Would you like to continue?

You have chosen to open Schedules only

The Schedules you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.

Would you like to continue?