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The Principles of Good Laboratory Practice (GLP) establish rules and criteria for a quality system that oversees the organizational processes and conditions in which non-clinical health and environmental safety studies are planned, conducted, monitored, recorded, reported, and archived.
WHO Good Clinical Laboratory Practice (GCLP) ISBN 978-92-4-159785-2; Stevens W. (2003) Good Clinical Laboratory Practice (GCLP): The need for a hybrid of Good Laboratory Practice and Good Clinical Practice guidelines/standards for medical testing laboratories conducting clinical trials in developing countries. Quality Assurance, 10: 83–89.
European Union: In the EU, Good Clinical Practice is backed and regulated by formal legislation contained in the Clinical Trial Regulation (Officially Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC). [3]
In fact, such predefined protocols are an essential component of Good Laboratory Practice (GLP) [11] and Good Clinical Practice (GCP) [12] [13] regulations. Protocols written for use by a specific laboratory may incorporate or reference standard operating procedures (SOP) governing general practices required by the laboratory. A protocol may ...
The CDC Good laboratory practice guidelines for newborn screening recommends that "laboratory specimen retention procedures should be consistent with patient decisions." [49] Researchers have described the NBS samples as a gold mine representing a patient population that would otherwise be impossible to get. [46]
"3. Good clinical laboratory practice (GCLP) for molecular based tests used in diagnostic laboratories". In Akyar, Isin (ed.). Wide Spectra of Quality Control. BoD – Books on Demand. pp. 29– 52. ISBN 978-953-307-683-6
Good agricultural practice; Good automated manufacturing practice; Good clinical data management practice; Good clinical laboratory practice; Good clinical practice; Good Clinical Practice Directive; Good documentation practice; Good engineering practice; Good manufacturing practice; Good safety practice; Good tissue practice
NATA represents Australia in a number of high-level International fora related to laboratory, inspection body, reference material producer and proficiency testing service provider accreditation practices and policies. NATA represents Australia through: the establishment of mutual recognition arrangements [8] with other accreditation bodies [9]