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Record keeping

Action for authorisation holders

If you are an authorisation holder under the GB Biocidal Products Regulation (GB BPR) you must keep records of the biocidal products you place on the GB market.

Records must be:

Action for biocidal product manufacturers

If you manufacture biocidal products that are placed on the GB market you must keep documentation relating to their quality and safety. The documentation may be held as paper or electronically and must include the following as a minimum:

In addition to the documentation, you must also store production batch samples. All documentation and samples must be made available to the enforcing authorities on request.

Updated 2021-03-29