Examples of using Laboratory practice in English and their translations into Polish
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Laboratory Practice.
More devices from common laboratory practice.
Good Laboratory Practice.
Research works are executed in line with Good Laboratory Practice GLP.
Good laboratory practice" What is behind all this?
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Certificates of compliance with Good Laboratory Practice shall accompany relevant studies.
Good laboratory practice" What is behind all this? PDF 246.32 kB.
It is only since the 1990s cultivation in the airspace have been widely used in laboratory practice.
Customer laboratory practice was also improved with valuable input given by Metrohm titration experts.
The history of great science, as well as everyday laboratory practice, knows many such situations.
Good laboratory practice for the purposes of mutual acceptance of data for the evaluation of chemical products; and.
Transportation-related pollution in the future can be simulated laboratory practice faithfully DUO LAB.
GLP(Good Laboratory Practice) requires, among other things, periodic checking of the analytical instruments for their reproducibility and correctness on the basis of Standard Operating Procedures SOPs.
Author of industry publications and speeches related to good design practice, as well as good laboratory practice.
Since 2003 all work in thePharmacology Departmenthas been done in accordance with Good Laboratory Practice, which has been recognized by means of GLP certificates issued by the Bureau for Chemical Substances Certificate no 6/2016/DPL.
Concerning the old approach legislation, implementation of the acquis on good laboratory practice has advanced.
Whereas it is indispensable to apply the principles of good laboratory practice when developing additives intended for use in feedingstuffs to ensure that the results of laboratory tests are not disputed; whereas recourse to procedures involving the use of laboratory animals for experimental or other scientific purposes should be kept to a minimum;
Whereas the resources devoted to the tests must not be wasted by having to repeat tests owing to differences in laboratory practice from one Member State to another;
COMMISSION DIRECTIVE 1999/11/EC of 8 March 1999 adapting to technical progress the principles of good laboratory practice as specified in Council Directive 87/18/EEC 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 Text with EEA relevance.
Coordinating the verification of compliance with the principles of good manufacturing practice, good laboratory practice and good clinical practice; .
The assessment of the safety for human health referred to in paragraph 1(d) shall be carried out in accordance with the principle of good laboratory practice laid down in Council Directive 87/18/EEC of 18 December 1986 on the harmonization of laws, regulations and administrative provisions relating to the application of the principles of good laboratory practice and the verification of their application for tests on chemical substances.
The above-mentioned methodologies of analysisof questionnaire results and audit were the original solution in terms of risk undertaken subject in laboratory practice.
Pharmacological tests, toxicological tests, residue tests andsafety tests shall be carried out in conformity with the provisions related to good laboratory practice(GLP) laid down in Directive 2004/10/EC of the European Parliament and of the Council1 and Directive 2004/9/EC of the European Parliament and of the Council2.
Whereas the Council of the Organization for Economic Cooperation and Development(OECD) took a Decision on 12 May 1981 on the mutual acceptance of data for the evaluation of chemical products;whereas it issued a recommendation on 26 July 1983 concerning the mutual recognition of compliance with good laboratory practice;
Even in recent scientific publications, one can very rarely find a declaration of compliance(or non-compliance)with good laboratory practice by the laboratories carrying out the relevant tests.
Where Community provisions require application of the principles of good laboratory practice following the entry into force of this Directive for tests on chemical products, Member States may not, on grounds relating to the principles of good laboratory practice, prohibit, restrict or impede the placing on the market of chemical products if the principles applied by the laboratories concerned are in conformity with those mentioned in Article 1.
Pharmacological, toxicological, residue andsafety tests shall be carried out in conformity with the provisions related to good laboratory practice(GLP) laid down in Directive 2004/10/EC and Directive 2004/9/EC.
Whereas for tests on chemical substances to be carried out in the context of this Regulation it is necessary to follow the good laboratory practices set out in Council Directive 87/18/EEC of 18 December 1986 on the harmonization of laws, regulations andadministrative provisions relating to the application of the principles of good laboratory practice and the verification of their application for tests on chemical substances(6);
GMO applicants are required to provide EFSA with specified studies which have to comply withEU/OECD study protocols and be performed under a given quality assurance system(Good Laboratory Practice or ISO) and in accordance with EFSA's guidance for the risk assessment of GMOs.
Whereas the introductions to the Annexes II andIII currently refer to the application of the principles of good laboratory practice(GLP) for any data requirements; whereas, however, the application of such principles is not considered to be appropriate for efficacy testing and for the testing of certain physico-chemical properties or other information which are not related to data on the properties and/or safety with respect to human or animal health or the environment;