Good laboratory practice (GLP) (English: Good Laboratory Practice) is a formal framework for the execution of safety examinations of chemical products. In many countries the GLP is legally prescribed.

The GLP puts the organizational operational sequence and the conditions, on which laboratory tests are planned, accomplished and supervised, firmly. Besides they are occupied also with the recording and reporting of the examination.

When consequence of the increasing health and environmental protection became in the past years a set of legal regulations discharged, to examine with the goal, chemical materials before their employment for their hazard potential for humans, animal and environment. All too uncritical handling medicine, plant protection agents as well as chemicals in the broadest sense, also in connection with a constantly growing employment at home or at the job, had well-known-measured again and again dangers for our health and our environment caused.

"„Property laboratory practice (GLP) is a quality assurance system, which concerned with the organizational operational sequence and the basic conditions, under which non-clinical health and environmentalrelevant safety examinations are planned, accomplished and supervised, as well as with the recording, archiving and reporting of the examinations. "“

The principles of the GLP represent thereby a safety framework for the quality of the chemico-physical, toxicological and examinations. With GLP the reliability of the data submitted at the evaluation authorities is to be ensured. GLP helps in this way to improve the quality of test data. Only a comparable quality of these data forms the basis for the mutual acknowledgment. The chemical law prescribes the adherence to the GLP not only for industrial chemicals, but seized also further chemical substances as well as materials of biological origin and its ranges of application. Under the obligation for adherence to the principles of the GLP all non-clinical examinations e.g. in the context the chemical-set fall by the evaluation authorities to be demanded in each case at the time of their execution.

Articles in category "Good Laboratory Practice"

We found here 8 articles.

Related Websites

We found here 6 related websites.

• FDA/ORA Compliance Program Guidance: GLP Supporting Documents
  Portal page to Good Laboratory Practices supporting documents, Q&A, ammendments, ... 7348.001 In-Vivo Bioequivalence · 7348.808 Good Laboratory Practice ...


• Good Laboratory Practice:Department
  The primary objective of the OECD Principles of GLP is to ensure the generation of high quality and reliable test data related to the safety of industrial ...


• OECD PRINCIPLES OF GOOD LABORATORY PRACTICE
  Studies covered by Good Laboratory Practice also include work conducted in field ... Good Laboratory Practice (GLP) is concerned with the organisational ...


• OECD Series on Principles of Good Laboratory Practice and ...
  The OECD Series on the Principles of Good Laboratory Practice and Compliance Monitoring comprises of guidance documents on various issues relating to Good ...


• TDR Publications: Good Laboratory Practice (GLP) Training Manual ...
  A tool for training and promoting good laboratory practice (GLP) ... This manual provides resource material for good laboratory practice (GLP) training. ...


• The Analytical Chemistry Springboard - Good Laboratory Practice ...
  The OECD Principles of GLP were first published in 1982 in Good Laboratory Practice in the Testing of Chemicals (OECD, 1982, out of print). ...