TY  - JOUR
AB  - The objective of this paper is to critique emerging legislation in the pharmaceutical industry, focusing on the clinical trials sector. Possible changes are identified and discussed in relation to their impact on phase I clinical trials conducted in the UK. It is concluded that smaller contract research organisations, which have benefited in the past from European Union legislative variation, may have resource problems in trying to cope with the changing business environment created through legislative harmonization. These SMEs must use this opportunity to seek clinical trials research partnerships in a new harmonized EU market.
VL  - 17
IS  - 7
SN  - 0952-6862
DO  - 10.1108/09526860410563195
UR  - https://doi.org/10.1108/09526860410563195
AU  - Murray Elizabeth
AU  - McAdam Rodney
AU  - Burke Moira T.
PY  - 2004
Y1  - 2004/01/01
TI  - A critique of emerging European legislation in the pharmaceutical industry: a clinical trials analysis
T2  - International Journal of Health Care Quality Assurance
PB  - Emerald Group Publishing Limited
SP  - 389
EP  - 393
Y2  - 2024/04/20
ER  -