Relevant bibliographies by topics / Good clinical laboratory practices

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Good clinical laboratory practices'

Author: Grafiati
Published: 7 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Good clinical laboratory practices"

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Selvakumar, R. "Good Laboratory Practices." Indian Journal of Clinical Biochemistry 25, no. 3 (2010): 221–24. http://dx.doi.org/10.1007/s12291-010-0077-z.

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Guindo, Merepen A., Renion Saye, Ruth D. Ellis, et al. "Promoting Good Clinical Laboratory Practices and Laboratory Accreditation to Support Clinical Trials in Sub-Saharan Africa." American Journal of Tropical Medicine and Hygiene 86, no. 4 (2012): 573–79. http://dx.doi.org/10.4269/ajtmh.2012.11-0691.

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Avani, Reddy Alla, T. Cherian Kevin, Surapaneni Ramya, et al. "IMPLEMENTATION OF GOOD LABORATORY PRACTICE IN PHARMACEUTICAL QUALITY CONTROL." International Journal of Current Pharmaceutical Review and Research 13, no. 4 (2021): 38–41. https://doi.org/10.5281/zenodo.12666981.

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Good Laboratory Practice (GLP) is a quality assurance system that sets forth guidelines andprinciples for the conduct of non-clinical laboratory studies. It encompasses a set ofstandardized practices and procedures that ensure the reliability, integrity, and validity of datagenerated during research and testing in various scientific fields, including pharmaceuticals,chemicals, agrochemicals, and cosmetics. Adhering to GLP promotes the generation of highquality and reliable data, enhances the credibility of scientific research, and contributes to thesafety and efficacy of products developed and
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Zhang, Helen L., Michael W. Omondi, Augustine M. Musyoka, et al. "Challenges of Maintaining Good Clinical Laboratory Practices in Low-Resource Settings." American Journal of Clinical Pathology 146, no. 2 (2016): 199–206. http://dx.doi.org/10.1093/ajcp/aqw083.

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Ravinetto, Raffaella, Emilie Alirol, Yodi Mahendradhata, et al. "Clinical Research in Neglected Tropical Diseases: The Challenge of Implementing Good Clinical (Laboratory) Practices." PLOS Neglected Tropical Diseases 10, no. 11 (2016): e0004654. http://dx.doi.org/10.1371/journal.pntd.0004654.

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Veit, Markus. "Good Clinical, Laboratory and Manufacturing Practices. Von Philip Carson, Nigel Dent (Editors)." Pharmazie in unserer Zeit 37, no. 4 (2008): 341. http://dx.doi.org/10.1002/pauz.200890056.

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Dugal, Robert. "Quality assurance and good laboratory practices in analytical doping control." Fresenius' Zeitschrift für analytische Chemie 330, no. 4-5 (1988): 337–38. http://dx.doi.org/10.1007/bf00469259.

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Dent, N. J. "European Regulatory Compliance Issues: Good Research Practices." Journal of the American College of Toxicology 13, no. 1 (1994): 79–85. http://dx.doi.org/10.3109/10915819409140658.

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Since the inception of the 1976 Food and Drug Administration (FDA) regulations governing preclinical toxicology, the world has seen an explosion of guidelines, principles, and regulations. The objective of this report is to clarify the situation in Europe as to the status of Good Laboratory Practices (GLPs). An overview of the harmonisation currently underway in Europe is given, although this changes frequently with new countries applying to join the European Community (EC) or undertaking aspects of GLP compliance. Where interactions have occurred between the GLPs and Good Clinical Practices (
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Kavsak, Peter A., and Catherine A. Hammett-Stabler. "Clinical Biochemistry year in review — The clinical “good”, the analytical “bad”, and the “ugly” laboratory practices." Clinical Biochemistry 47, no. 18 (2014): 255–56. http://dx.doi.org/10.1016/j.clinbiochem.2014.11.015.

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Ibrahim, Faisal, David Dosoo, Karl C. Kronmann, et al. "Good Clinical Laboratory Practices Improved Proficiency Testing Performance at Clinical Trials Centers in Ghana and Burkina Faso." PLoS ONE 7, no. 6 (2012): e39098. http://dx.doi.org/10.1371/journal.pone.0039098.

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Dissertations / Theses on the topic "Good clinical laboratory practices"

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Hanna, Mina. "Indicateurs de qualité des essais cliniques dans les pays du sud : consensus et étude de faisabilité dans les essais de l’ANRS." Thesis, Bordeaux 2, 2012. http://www.theses.fr/2012BOR21993/document.

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Depuis 1994, l’ANRS mène en tant que promoteur des études cliniques dans les pays à ressources limitées. Ces études sur le Sida et les hépatites virales sont principalement menées dans les huit sites de l’agence en Afrique Subsaharienne, au Moyen Orient, en Asie du Sud-Est et en Amérique Latine. Les chercheurs dans les pays à ressources limitées font face à deux problématiques majeures : (i) les règles des Bonnes Pratiques Cliniques (BPC) n’intègrent pas leurs particularités fonctionnelles et culturelles ; et (ii) aucun outil n’existe dans la littérature pour évaluer l’adhésion des études clin
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Zambonato, Bruna Pochmann. "Boas práticas clínicas e aspectos regulatórios em pesquisas com terapia celular." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2016. http://hdl.handle.net/10183/151496.

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No campo da pesquisa clínica, o manual de Boas Práticas Clínicas (BPC) é um padrão de qualidade que garante não só que a segurança, os direitos e o bem-estar dos participantes destes estudos sejam protegidos, mas também que a credibilidade e precisão dos dados sejam garantidas. Com o avanço das pesquisas envolvendo terapia celular (TC), são necessários a mesma atenção e acompanhamento dado a ao estudo clínico envolvendo fármacos. Além disso, é necessário que a TC trabalhe de acordo com as Boas Práticas de Manufatura (BPM) desenvolvendo um alto padrão de qualidade para produção celular. O objet
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Couto, Marcus Vinicius Lima do. "A Pré-Qualificação de medicamentos: análise comparativa entre as Boas Práticas de Fabricação da OMS e da ANVISA." reponame:Repositório Institucional da FIOCRUZ, 2014. https://www.arca.fiocruz.br/handle/icict/11632.

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Made available in DSpace on 2015-08-19T13:52:56Z (GMT). No. of bitstreams: 2 15.pdf: 2031861 bytes, checksum: 32edc08872af428837658b461b80f2a7 (MD5) license.txt: 1748 bytes, checksum: 8a4605be74aa9ea9d79846c1fba20a33 (MD5) Previous issue date: 2014<br>Fundação Oswaldo Cruz. Instituto de Tecnologia em Fármacos/Farmanguinhos. Rio de Janeiro, RJ, Brasil.<br>A produção de medicamentos com qualidade, segurança, eficácia é fundamental para atender às demandas nacionais e internacionais, com o fito de subsidiar a assistência farmacêutica no âmbito da saúde pública. Diante do papel estratégico em
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Marques, Tiago Emanuel Domingues Costa. "Curricular training report at W4Research: contract research organization." Master's thesis, Universidade de Aveiro, 2016. http://hdl.handle.net/10773/17082.

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Mestrado em Biomedicina Farmacêutica<br>O presente relatório destina-se a descrever as atividades desenvolvidas no âmbito do estágio curricular que teve lugar na W4Research, uma Contract Research Organization (CRO). O estágio teve a duração de 8 meses durante os quais o estagiário desempenhou funções de CRA sendo o principal foco a monitorização de estudos observacionais. Para além da principal atividade, foram ainda desenvolvidas funções em áreas adjacentes à investigação clínica, tais como, o Medical Writing e a gestão da qualidade. Este trabalho pretende mostrar a visão obtida e os pontos
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Almas, Magda Sofia Falé. "Formação em contexto de trabalho em laboratório da indústria farmacêutica." Master's thesis, 2021. http://hdl.handle.net/10400.26/37077.

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O presente relatório descreve as atividades desenvolvidas no âmbito do estágio curricular do Mestrado em Engenharia Biológica e Química na Escola Superior de Tecnologia do Barreiro e decorreu na Indústria Farmacêutica Generis, S.A., de março a julho de 2021. O estágio tinha como objetivo, permitir aplicar os conhecimentos teóricos adquiridos, em contexto real, dando à discente as competências necessárias. Neste estágio, a discente aprendeu a trabalhar sob as regras de Boas práticas de fabricação/ Good Manufacturing Practices (GMPs) que descrevem o padrão mínimo de que um fabrican
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Ladeiro, Joana Gomes. "Critérios para um Centro de Investigação Clínica de Referência." Master's thesis, 2020. http://hdl.handle.net/10316/93001.

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Dissertação de Mestrado em Farmacologia Aplicada apresentada à Faculdade de Farmácia<br>Clinical research is essential for advancing scientific knowledge and improving society's quality of life.Clinical studies are a key process in the clinical research value chain as they provide high levels of evidence and significant results about drugs, medical devices, health data, safety of interventions or health services.All clinical studies require quality and safety guarantees oriented mainly to the patient, which requires multidisciplinary coordination based on meeting the needs of citizens and supp
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Pires, Elisabete Andrade Alves. "Professional activity report." Master's thesis, 2014. http://hdl.handle.net/10362/17638.

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Maia, Morgana Monteiro. "Boas Práticas de Fabrico em Medicamentos Experimentais." Master's thesis, 2019. http://hdl.handle.net/10316/88205.

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Dissertação de Mestrado em Biotecnologia Farmacêutica apresentada à Faculdade de Farmácia<br>As Boas Práticas de Fabrico BPF (ou, no inglês) GMP, Good Manufacturing Pratices são definidas como normas responsáveis por garantir a qualidade, segurança e eficácia dos medicamentos, e baseiam-se em alguns princípios básicos para a minimização de riscos. Surgiram como iniciativa da Organização Mundial da Saúde (OMS) em 1968.Ao longo de todos estes anos, as indústrias farmacêuticas têm presenciado drásticas alterações no que diz respeito às BPF, de modo a criar requisitos de qualidade sólidos e a melh
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Silva, Maria Gabriela Freitas da. "From Lab to Large-Scale Development of Clinically Compliant Nanopharmaceutics." Master's thesis, 2017. http://hdl.handle.net/10316/83699.

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Dissertação de Mestrado em Tecnologias do Medicamento apresentada à Faculdade de Farmácia<br>Os maiores desafios encontrados durante o desenvolvimento de nanofarmacêuticos estão relacionados com a sua estabilidade a longo prazo e a produção em larga escala de formulações adequadas para o uso em ensaios clínicos. Assim como a falta de harmonização no que diz respeito à sua regulação. Nesta revisão são abordadas as boas práticas de fabrico (BPF) que podem ser aplicadas à produção de nanofarmacêuticos, desde a escala piloto até à escala industrial, de modo a que possam ser usados em ensaios clíni
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Books on the topic "Good clinical laboratory practices"

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Carson, Philip, and Nigel Dent, eds. Good Clinical, Laboratory and Manufacturing Practices. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557728.

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1944-, Carson P. A., Dent N. J, and Royal Society of Chemistry (Great Britain), eds. Good clinical, laboratory and manufacturing practices: Techniques for the QA professional. RSC, 2007.

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1944-, Carson P. A., and Dent N. J, eds. Good laboratory and clinical practices: Techniques for the quality assurance professional. Heinemann Newnes, 1990.

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Schnoll, Les. The regulatory compliance almanac: A guide to good manufacturing, clinical, and laboratory practices. Paton Professional, 2008.

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Garner, Willa Y., and Maureen S. Barge, eds. Good Laboratory Practices. American Chemical Society, 1988. http://dx.doi.org/10.1021/bk-1988-0369.

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Bunn, Graham P. Good Clinical Practices in Pharmaceuticals. CRC Press, 2024. http://dx.doi.org/10.1201/9781003407010.

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Catalano, Thomas. Good Laboratory Practices for Forensic Chemistry. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-09725-1.

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E, Stewart Charles. Basic quality assurance practices for clinical laboratories. Van Nostrand Reinhold, 1989.

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Cervenka, Nicole, ed. Implementation of Good Laboratory Practices: A Joint Pakistan-U.S. Workshop. National Academies Press, 2020. http://dx.doi.org/10.17226/25967.

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Bohaychuk, W. Good clinical research practices: Standard operating procedures for investigators : a manual. 2nd ed. Good Clinical Research Practices, 1993.

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Book chapters on the topic "Good clinical laboratory practices"

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Ford, P. J. "Chapter 11. Clinical Laboratories." In Good Clinical, Laboratory and Manufacturing Practices. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557728-00147.

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Talbot, D., and N. Downes. "Chapter 1. Introduction: Good Clinical Practice." In Good Clinical, Laboratory and Manufacturing Practices. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557728-00001.

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Helder, Th. "Chapter 12. Introduction: Good Laboratory Practice." In Good Clinical, Laboratory and Manufacturing Practices. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557728-00169.

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Bailes, D. "Chapter 8. Good Clinical Practice/Good Manufacturing Practice (GCP/GMP) Interface, Investigational Product Accountability." In Good Clinical, Laboratory and Manufacturing Practices. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557728-00109.

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Dolman, J. R. "Chapter 26. Introduction: Good Manufacturing Practice." In Good Clinical, Laboratory and Manufacturing Practices. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557728-00369.

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Benton, M. J. "Chapter 20. Good Laboratory Practice and Pharmacology." In Good Clinical, Laboratory and Manufacturing Practices. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557728-00271.

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Lange-Asschenfeldt, Christian. "Good Clinical and Good Laboratory Practice (GCP)." In Encyclopedia of Sciences and Religions. Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-1-4020-8265-8_200800.

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Dent, N. J. "Chapter 2. The Protocol, Case Report Form and Initial Documentation: Quality Assurance Involvement and Common Problems." In Good Clinical, Laboratory and Manufacturing Practices. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557728-00013.

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Nickols, P. Charnley, and J. Nickols. "Chapter 3. Standard Operating Procedures in the Good Clinical Practice Environment." In Good Clinical, Laboratory and Manufacturing Practices. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557728-00039.

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Brown, E. G., and S. A. Goldman. "Chapter 4. Preparing for Regulatory Inspection of Company Pharmacovigilance Systems and Practices in the European Union and United States." In Good Clinical, Laboratory and Manufacturing Practices. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557728-00057.

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Conference papers on the topic "Good clinical laboratory practices"

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Ampudia-Blasco, Francisco Javier, Alba Cuerda-del Pino, Sergio Martínez-Hervás, Jordi Ferri Císcar, and José Tomás Real Collado. "NEW VIRTUAL CLINICAL PRACTICES WITH VIDEO STREAMING TO PROMOTE GOOD CLINICAL PRACTICES IN MEDICAL EDUCATION." In 17th International Conference on Education and New Learning Technologies. IATED, 2025. https://doi.org/10.21125/edulearn.2025.1281.

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Steely, Carroll N. "The Effects of Overvoltage When Applied to a Dielectric Film to Evaluate Cathodic Disbondment and Potential Performance by Means of Accelerated Laboratory Test Conditions." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90251.

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Abstract There is considerable evidence and historical data to support the position that laboratory tests conducted on candidate coatings at overvoltage values to ascertain adhesion and expected performance characteristics are misleading and unreliable, and in many cases screen out many field-proven, reliable coatings to the detriment of the user. Further, that the users spend considerable sums of money replacing coatings or tapes that looked good in the lab but fared badly in service because they are excellent electrical insulators but poor corrosion-resistant barriers. Finally, because of po
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Lolla, T., J. Siefert, H. Lee, et al. "Understanding the Kinetics of Sigma Phase Evolution in Super 304H using Lab Creep Tested Heats and Long-term Service Aged Components." In AM-EPRI 2024. ASM International, 2024. http://dx.doi.org/10.31399/asm.cp.am-epri-2024p0635.

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Abstract Super 304H is a new generation of advanced austenitic stainless steels that is increasingly being used in superheater/ reheater (SH/RH) sections of thermal ultra-supercritical steam power plants due to its high creep strength combined with good oxidation resistance and microstructure stability. However, recent studies have shown significant microstructural changes and associated degradation in creep performance during long-term service exposure in this alloy. Microstructure evolution during service and its effect on the long-term creep performance has not been comprehensively assessed
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Arakere, Ajay, Marlane Rodriguez, Dirk Oostendorp, Prasanna Swamy, Robert McStravick, and Alex Bridges. "An Approach to Optimize the Wall Thickness of In-Service Pipelines." In CORROSION 2021. AMPP, 2021. https://doi.org/10.5006/c2021-16885.

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Abstract This paper presents a case study of a hypothetical pipeline that operated without coatings or Cathodic Protection (CP) for nearly the first 20 years of its service. Metal loss anomalies with depths greater than 50% of nominal wall thickness will require excavation according to federal regulations. To reduce the number of unnecessary excavations, laboratory testing data combined with methodology from both API 579 and ASME B31.4 was applied to determine an optimized wall thickness (t’). Based on hypothetical anomaly data considered in this paper, the optimized wall thickness resulted in
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Castaneda, H., Lin Chen, Hui Wang, and Sreelakshmi Sreeharan. "Classification of Active and Passive Surface Conditions Based on Different Relaxation Response for External Corrosion Coated Pipelines." In CONFERENCE 2022. AMPP, 2022. https://doi.org/10.5006/c2022-18052.

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Abstract The energy transportation network of the United States consists of over 2.5 million miles of buried pipelines. It is of prime importance the integrity of the metallic assets due to degradation in soil conditions because of their constant exposure to the aggressive, dynamic, and heterogeneous environment. This degradation process, involves a sequence of process starting with the coating damages/failures and the following electrochemical reactions. External corrosion can result in gradual and usually localized metal loss on the exterior surface of failure coating, resulting in reduction
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LeBeau, Stephen, Raymond Decker, Charles Sfeir, and Boyce Collins. "Controlling the Degradation Profile of Mg Biomedical Devices by Alloy Design and Thermomechanical Processing." In CORROSION 2017. NACE International, 2017. https://doi.org/10.5006/c2017-09395.

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Abstract Magnesium (Mg) alloys are gaining interest for biodegradable medical implant devices due to a good combination of mechanical properties and biocompatibility. Nevertheless, the fast degradation rates of Mg and its biocompatible alloys in the aggressive physiological environment impose limitations on their clinical applications. This necessitates the development of Mg based implants with controlled degradation rates to match the kinetics of the bone and tissue healing process and to avoid any complications or issues that might negatively impact surrounding tissues. The current study pre
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"QUALITY OF CLINICAL LABORATORY SERVICES IN A TERTIARY HEALTH CARE FACILITY, IBADAN NORTH LOCAL GOVERNMENT AREA, IBADAN." In International Conference on Public Health and Humanitarian Action. International Federation of Medical Students' Associations - Jordan, 2022. http://dx.doi.org/10.56950/hxts1913.

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Background: Quality clinical laboratory service provision is very important in order to enhance diagnostic value and improve the health status of the community. However, there is very little information on the actual standard adaptation, and implementation, or the impact policy guidelines have had on laboratory services delivery and the community. This study assessed the quality of clinical laboratory services in a tertiary health care facility in Ibadan North Local Government Area, Oyo state. Methods: Interview was conducted for 125 laboratory staff and 426 patients. Five laboratory units wer
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Fonseca, Pedro, Ricardo Vigário, Ana Teresa Videira Gabriel, Isabel L. Nunes, Carla Quintão, and Cláudia Quaresma. "Validation of a rehabilitation platform for visuomotor perceptual and cognitive stimulation." In 14th International Conference on Applied Human Factors and Ergonomics (AHFE 2023). AHFE International, 2023. http://dx.doi.org/10.54941/ahfe1003595.

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Stroke, or cerebrovascular accident, is a major global health problem and one of the leading causes of death and acquired disability worldwide. After a stroke, deficits in perceptual and cognitive functions may arise, with particular emphasis to impairments caused to visuomotor skills. In this way, its stimulation, within a therapeutic rehabilitation context, is truly relevant for the recovery of lost functions. RehabVisual, presented in earlier works, is a digital platform that allows for an objective and standardized assessment of visuomotor skills and specific clinical interventions for eac
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Ampudia-Blasco, Francisco Javier, Sergio Martínez-Hervás, Alba Cuerda del Pino, Jordi Ferri Císcar, and José Tomás Real Collado. "VIRTUAL CLINICAL PRACTICES WITH VIDEO STREAMING TO PROMOTE GOOD CLINICAL PRACTICES AND HUMANISM IN MEDICINE." In 16th International Conference on Education and New Learning Technologies. IATED, 2024. http://dx.doi.org/10.21125/edulearn.2024.1497.

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"EVALUATION OF THE ASSESSMENT DOSE WITH BIODOSIMETRY METHODS, APPLICABLE IN BULGARIA. USE OF DICENTRIC CHROMOSOMAL ASSAY (DCA) AND CYTOKINESIS-BLOCK MICRONUCLEUS ASSAY." In RAD Conference. RAD Centre, Niš, Serbia, 2024. https://doi.org/10.21175/radproc.2024.08.

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Radiation biodosimetry deals with the measurement of a biological response that serves as a surrogate for estimating the absorbed radiation dose in exposed humans. The biodosimetry methods include cytogenetic methods such as dicentric chromosomal assay (DCA), cytokinesis-block micronucleus assay (CBMN), Fluorescence in-situ hybridization (FISH) assay, Premature chromosome condensation (PCC), etc. All of them score the marking damages such dicentric chromosomes or centric rings to calculate the absorbed dose of ionizing radiation. As a part of the European union, Bulgarian radiobiology laborato
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Reports on the topic "Good clinical laboratory practices"

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Iveson, Steven W. Good Manufacturing Practices (GMP) / Good Laboratory Practices (GLP) Review and Applicability for Chemical Security Enhancements. Office of Scientific and Technical Information (OSTI), 2014. http://dx.doi.org/10.2172/1259847.

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Schmidt-Sane, Megan, Samantha Vanderslott, Hana Rohan, and Luisa Enria. Key Considerations: Using Social and Behavioural Science to Inform the Use of Vaccines During Health Emergencies. Institute of Development Studies, 2025. https://doi.org/10.19088/sshap.2025.013.

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This brief synthesises social and behavioural science (SBS) research on the use of vaccines during health emergencies in sub-Saharan Africa, including vaccines undergoing clinical trials (‘experimental vaccines’). There are outbreaks of mpox, Marburg virus disease and Ebola (Sudan virus disease) in the region, and multiple clinical trials of vaccines for these diseases are in progress. Findings from SBS research can contribute to strategies to build confidence in vaccines and, importantly, the design of clinical trials and vaccine roll-out. To improve effective vaccine roll-out, it is critical
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Bellissant, Eric, Isabelle Boutron, Carole Chapin, et al. Ensuring that the results of all clinical trials in France are posted. Ministère de l’enseignement supérieur et de la recherche, 2025. https://doi.org/10.52949/56.

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The Working Group on “Transparency and the publicising of the results of health research”, was appointed by the French Ministry in charge of Research, in conjunction with the French Ministry in charge of Health. It seeks to address the problem of publication bias, which is the tendency to prioritise the publication of positive results. However, if they are based on an incomplete, skewed understanding of research results, this bias may result in erroneous health policy decisions. This report makes recommendations towards all stakeholders involved in clinical research, and covers the entire scie
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McCarthy, Sean T., Aneesa Motala, Emily Lawson, and Paul G. Shekelle. Prevention in Adults of Transmission of Infection With Multidrug-Resistant Organisms. Rapid Review. Agency for Healthcare Research and Quality (AHRQ), 2024. http://dx.doi.org/10.23970/ahrqepc_mhs4mdro.

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Objectives. This rapid review summarizes literature for patient safety practices intended to prevent and control the transmission of multidrug-resistant organisms (MDROs). Methods. We followed rapid review processes of the Agency for Healthcare Research and Quality Evidence-based Practice Center Program. We searched PubMed to identify eligible systematic reviews from 2011 to May 2023 and primary studies published from 2011 to May 2023, supplemented by targeted gray literature searches. We included literature that addressed patient safety practices intending to prevent or control transmission o
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Bray, Jonathan, Ross Boulanger, Misko Cubrinovski, et al. U.S.—New Zealand— Japan International Workshop, Liquefaction-Induced Ground Movement Effects, University of California, Berkeley, California, 2-4 November 2016. Pacific Earthquake Engineering Research Center, University of California, Berkeley, CA, 2017. http://dx.doi.org/10.55461/gzzx9906.

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Abstract:
There is much to learn from the recent New Zealand and Japan earthquakes. These earthquakes produced differing levels of liquefaction-induced ground movements that damaged buildings, bridges, and buried utilities. Along with the often spectacular observations of infrastructure damage, there were many cases where well-built facilities located in areas of liquefaction-induced ground failure were not damaged. Researchers are working on characterizing and learning from these observations of both poor and good performance. The “Liquefaction-Induced Ground Movements Effects” workshop provided an opp
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