Results 261 to 270 of about 1,091,889 (296)
Some of the next articles are maybe not open access.
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
openaire +3 more sources
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
GOOD CLINICAL PRACTICE IN CLINICAL RESEARCH
The Lancet, 1989S L, Nightingale, F O, Kelsey
openaire +4 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.
openaire +1 more source
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.
openaire +1 more source
ESHRE good practice recommendations on recurrent implantation failure
Human Reproduction Open, 2023Danilo Cimadomo +2 more
exaly
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
openaire +1 more source
Good publication practice for pharmaceutical companies
Current Medical Research and Opinion, 2003Elizabeth Wager
exaly
ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders†
Human Reproduction Open, 2020Felix Carvalho +2 more
exaly