Results 251 to 260 of about 14,696,344 (291)
Some of the next articles are maybe not open access.
2010
Good Clinical Practice (GCP) is an internationally recognized standard governing the ethical and scientific quality for the design, conduct, recording and reporting of clinical trials involving human subjects. While full compliance with each of the principles of ICH GCP is not mandatory for the conduct of cosmetic studies, the spirit of GCP should be ...
Mamoru Narukawa, Masahiro Takeuchi
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Good Clinical Practice (GCP) is an internationally recognized standard governing the ethical and scientific quality for the design, conduct, recording and reporting of clinical trials involving human subjects. While full compliance with each of the principles of ICH GCP is not mandatory for the conduct of cosmetic studies, the spirit of GCP should be ...
Mamoru Narukawa, Masahiro Takeuchi
+5 more sources
Der Urologe A, 2000
The term Good Clinical Practice (GCP) suggests that it relates to a standard of practical clinical medicine; it does not. It is a standard, or more precisely, a set of standards that have been developed for the conduct of clinical trials with investigative new drugs. These standards can actually be applied to any experimentation in humans.
Jean Soul-Lawton, Ria Kroon
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The term Good Clinical Practice (GCP) suggests that it relates to a standard of practical clinical medicine; it does not. It is a standard, or more precisely, a set of standards that have been developed for the conduct of clinical trials with investigative new drugs. These standards can actually be applied to any experimentation in humans.
Jean Soul-Lawton, Ria Kroon
openaire +2 more sources
Putting the “good” into Good Clinical Practice
Medical Journal of Australia, 2021Symons, T, Webb, S, Zalcberg, JR
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Good Clinical Practices in the Bioanalytical Laboratory
Bioanalysis, 2023Despite the existence of good clinical practice guidelines, the way in which they are applied to the bioanalytical laboratory remains unclear. Aspects of patient confidentiality, informed consent and subject withdrawal; addressing unblinding associated with sample analysis, including repeat analysis and incurred sample reanalysis; or the differences in
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Nuclear Medicine Communications, 2005
Radiopharmaceuticals account for more than 95% of the group of sterile pharmaceutical products and should therefore be handled and produced with care. Since the introduction of the European directive, all pharmaceuticals used in clinical studies must be prepared under good manufacturing practice (GMP) conditions. This review aims to give an overview of
De Vos, FJ, De Decker, M, Dierckx, RA
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Radiopharmaceuticals account for more than 95% of the group of sterile pharmaceutical products and should therefore be handled and produced with care. Since the introduction of the European directive, all pharmaceuticals used in clinical studies must be prepared under good manufacturing practice (GMP) conditions. This review aims to give an overview of
De Vos, FJ, De Decker, M, Dierckx, RA
openaire +3 more sources
1988
The title of this paper should really be ‘Good clinical research practice’, as the topic is concerned with the execution and evaluation of clinical research projects and not the routine diagnosis and treatment of individual patients under the care of their attending physician.
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The title of this paper should really be ‘Good clinical research practice’, as the topic is concerned with the execution and evaluation of clinical research projects and not the routine diagnosis and treatment of individual patients under the care of their attending physician.
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GOOD CLINICAL PRACTICE IN CLINICAL RESEARCH
The Lancet, 1989S L, Nightingale, F O, Kelsey
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Good laboratory practice and good clinical laboratory practice
Abstract Concepts of Good laboratory practice (GLP) and Good clinical laboratory practice (GCLP) are defined and explained, highlighting that research not conducted according to GLP standards is not normally included in the regulatory filings for licensing. However, exemptions exist where specialized testing systems are required.Phil Ambery +2 more
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