# Directive 2004/10/EC of the European Parliament and of the Council of 11 February 2004 on the harmonisation of laws, regulations and administrative provisions relating to the application of the principles of good laboratory practice and the verification of their applications for tests on chemical substances (codified version) (Text with EEA relevance), Division 8.2: Content of the study plan

Extent: E+W+S+N.I.

The study plan should contain, but not be limited to the following information:
1..
Identification of the study, the test item and reference item
(a) A descriptive title
(b) A statement which reveals the nature and purpose of the study
(c) Identification of the test item by code or name (IUPAC; CAS number, biological parameters, etc.)
(d) The reference item to be used.
2..
Information concerning the sponsor and the test facility
(a) Name and address of the sponsor
(b) Name and address of any test facilities and test sites involved
(c) Name and address of the study director
(d) Name and address of the principal investigator(s), and the phase(s) of the study delegated by the study director and under the responsibility of the principal investigator(s).
3..
Dates
(a) The date of approval of the study plan by signature of the study director. The date of approval of the study plan by signature of the test facility management and sponsor if required by national regulation or legislation in the country where the study is being performed.
(b) The proposed experimental starting and completion dates.
4..
Test methods
Reference to the OECD test guideline or other test guideline or method to be used.
5..
Issues (where applicable)
(a) The justification for selection of the test system
(b) Characterisation of the test system, such as the species, strain, substrain, source of supply, number, body weight range, sex, age and other pertinent information
(c) The method of administration and the reason for its choice
(d) The dose levels and/or concentration(s), frequency, and duration of administration/application;
(e) Detailed information on the experimental design, including a description of the chronological procedure of the study, all methods, materials and conditions, type and frequency of analysis, measurements, observations and examinations to be performed, and statistical methods to be used (if any).
6..
Records
A list of records to be retained.

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Source: https://www.legislation.gov.uk/eudr/2004/10/annex/I/section/II/division/8/division/8.2 (the official version)
Page: https://openlegislation.uk/eu-directive-2004-10/annex-I/section-II/division-8/division-8.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.