Biomedical Engineering Reference
In-Depth Information
O'Donnell, K., Greene, A. (2006) A risk management
solution designed to facilitate risk-based qualifi cation,
validation, and change control activities within GMP and
pharmaceutical regulatory compliance environments in
the EU, Parts I and II. J. GXP Comp. 10(4), July.
Ostrove, S. (2008) Qualifi cation and change control, in
Validation of Pharmaceutical Processes , 3rd edn,
J.P. Agalloco and F.J. Carleton (eds), New York: Informa
Healthcare, p. 130.
Scannell, E.E. (1992) We've got to stop meeting like this.
Train. Devel. 46(1), 71.
Shoenfelt, E., Pedigo, L. (2005) A review of court decisions
on cognitive ability testing, 1992-2004. Rev. Publ. Pers.
Admin. 25(3), 271-87.
Smalley, C. (2008) Validation of training, in Validation of
Pharmaceutical Processes , 3rd edn, J.P. Agalloco and
F.J. Carleton (eds), New York: Informa Healthcare,
pp. 523-8.
Weinberg, S., Fuqua, R. (2010) A stochastic model of 'quality
by design' for the pharmaceutical industry, presented at
the Pittsburgh Conference on Analytical Chemistry and
Applied Spectroscopy , Orlando, FL: PittCon, February/
March, p. 5.
￿ ￿ ￿ ￿ ￿
Search WWH ::




Custom Search