Centre for Medicines Research Workshop – serie
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9 produkter
Improving the Regulatory Review Process
Industry and Regulatory Initiatives
Av C. Lumley, S.R. Walker
Inbunden, 1996
1692 kr
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Regulatory review is the last major development hurdle that must be passed by a new medicine before it reaches the market. At a time when pharmaceutical companies are reviewing their R&D strategies, and attempting to reduce drug development times, it is extremely important that the review process …
Improving the Regulatory Review Process
Assessing Performance and Setting Targets
Av McAuslane, J. A. Neil McAuslane m. fl.
Inbunden, 1998
905 kr
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At a time when it is becoming usual for medicines to be developed for a global market and pharmaceutical companies are endeavouring to expedite the drug development process, Regulatory authorities are concentrating on improving their efficiency and effectiveness. Therefore, it is not surprising …
Safety Evaluation of Biotechnologically-derived Pharmaceuticals
Facilitating a Scientific Approach
Av Susan A. Griffiths, C. Lumley
Inbunden, 1998
1130 kr
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Considerable investment has been made by both pharmaceutical and biotechnology companies in pharmaceutical products of biotechnology. However, because relatively few of these products have been marketed, lack of relevant experience means that uncertainty still surrounds the most appropriate …
Relevance of Ethnic Factors in the Clinical Evaluation of Medicines
Medicines
Av Stuart Walker, J. A. Neil McAuslane m. fl.
Inbunden, 1994
905 kr
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There is currently limited acceptance of foreign clinical data by regulatory authorities, although the reasons for repeating studies are poorly defined. There are some proven genetic differences in drug metabolism and elimination which occur with varying frequencies in different populations. In …
Long-Term Animal Studies
Their Predictive Value for Man
Av S.R. Walker, Anthony D. Dayan
Inbunden, 1986
2252 kr
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Relevance of Ethnic Factors in the Clinical Evaluation of Medicines
Proceedings of a Workshop held at The Medical Society of London, UK, 7th and 8th July, 1993
Av S.R. Walker, C. Lumley m. fl.
Häftad, 2012
569 kr
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For a research-based pharmaceutical company to be successful in the 1990s. it must have a strategic plan for the global development of new chemical entities. Global development can be defined as an attempt to reach all major markets as rapidly as possible and for many companies these will include …
Improving the Regulatory Review Process: Assessing Performance and Setting Targets
Häftad, 2012
504 kr
Lägg i varukorg
At a time when it is becoming usual for medicines to be developed for a global market and pharmaceutical companies are endeavouring to expedite the drug development process, Regulatory Authorities are concentrating on improving their efficiency and effectiveness. Therefore, it is not surprising …
Safety Evaluation of Biotechnologically-derived Pharmaceuticals
Facilitating a Scientific Approach
Av Susan A. Griffiths, C. Lumley
Häftad, 2012
1002 kr
Lägg i varukorg
Considerable investment has been made by both pharmaceutical and biotechnology companies in pharmaceutical products of biotechnology. However, because relatively few of these products have been marketed, lack of relevant experience means that uncertainty still surrounds the most appropriate …
Improving the Regulatory Review Process
Industry and Regulatory Initiatives
Av C. Lumley, S.R. Walker
Häftad, 2011
1500 kr
Lägg i varukorg
Regulatory review is the last major development hurdle that must be passed by a new medicine before it reaches the market. At a time when pharmaceutical companies are reviewing their R&D strategies, and attempting to reduce drug development times, it is extremely important that the review process …
