Covers pre-clinical information relevant to early human studies, including pharmaceutical, metabolic, toxicological and regulatory aspects, as well as the general considerations relevant to early human studies. This work is suitable for industry and academic professionals involved in the development of new drugs.
Covers pre-clinical information relevant to early human studies, including pharmaceutical, metabolic, toxicological and regulatory aspects, as well as...
In recent years the need for specialist knowledge of the laws governing the regulation of medicines has become apparent. This is the case among not only lawyers but also hospitals, researchers, prescribers and many others involved in the provision of healthcare. Such a need has been precipitated by a number of factors including the changing structure of healthcare in the UK and Europe, the increasing specialisation in litigation relating to medicines' control and provision and the various changes in regulation that have arisen both from challenges in the courts and from the intervention of...
In recent years the need for specialist knowledge of the laws governing the regulation of medicines has become apparent. This is the case among not on...
In recent years the need for specialist knowledge of the laws governing the regulation of medicines has become apparent. This is the case among not only lawyers but also hospitals, researchers, prescribers and many others involved in the provision of healthcare. Such a need has been precipitated by a number of factors including the changing structure of healthcare in the UK and Europe, the increasing specialisation in litigation relating to medicines' control and provision and the various changes in regulation that have arisen both from challenges in the courts and from the intervention of...
In recent years the need for specialist knowledge of the laws governing the regulation of medicines has become apparent. This is the case among not on...
