# The Good Laboratory Practice Regulations 1997, Paragraph 19: Application


(1) Standard operating procedures should be available for, but not be limited to, the following categories of laboratory activities. The details given under each heading are to be considered as illustrative examples—
(a) Test and reference substances
receipt, identification, labelling, handling, sampling and storage;
(b) Apparatus and reagents
use, maintenance, cleaning, calibration of measuring apparatus and environmental control equipment; preparation of reagents;
(c) Record keeping, reporting, storage and retrieval
coding of studies, data collection, preparation of reports, indexing systems, handling of data, including the use of computerised data systems;
(d) Test system (where appropriate)
(i) room preparation and environmental room conditions for the test system,
(ii) procedures for receipt, transfer, proper placement, characterisation, identification and care of test system,
(iii) test system preparation, observation examinations before, during and at termination of the safety study,
(iv) handling of test system individuals found moribund or dead during the safety study,
(v) collection, identification and handling of specimens including necropsy and histopathol ogy;
(e) Quality assurance procedures
operation of quality assurance personnel in performing and reporting study audits, inspections and final study report reviews;
(f) Health and safety precautions
as required by national and/or international legislation or guidelines.

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Source: https://www.legislation.gov.uk/uksi/1997/654/schedule/1/paragraph/19 (the official version)
Page: https://openlegislation.uk/good-laboratory-practice-regulations-1997/schedule-1/paragraph-19
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.