Biomedical Engineering Reference
In-Depth Information
McDowell, R. (2004) Quo Vadis: 21 CFR 11. LC GC
Europe [Liquid Chromatography - Gas Chromatography],
17(2), 80-1.
Moore, C. (2007) Learning from key learning indicators.
Chief Learn. Off.
6(8), 39.
Myler, E. (2006) The ABCs of records retention schedule
development.
E-DOC Mag.
20(3), 52-6.
Phillips, J. (2007) Measuring the ROI of a coaching
intervention, Part 2.
Perf. Imp.
46(10), 10-23.
Phillips, J., Phillips, P. (2007) Show me the money: the use of
ROI in performance improvement, Part 1.
Perf. Imp.
46(9), October.
Riordan, D. (2007) How enterprise software facilitates FDA
compliance.
Qual. Dig.
27(12), December.
Schneier, B. (2005) Two-factor authentication.
Comm.
ACM
, 48(4), 136.
Shukla, R. (2004) The case for electronic records management.
Fin. Exec.
20(7), 50-2.
Stephenson, D. (2007) Accelerating compliance.
E-DOC
Mag.
21(4), 27-9.
Stolovitch, H.D. (2007) The story of training transfer.
Talent
Man. Mag.
3(9), 12.
Tennant, C., Boonkrong, M., and Roberts, P. (2002) The
design of a training programme measurement model,
J. Europ. Ind. Trg.
26(5), 230-40.
Torres, T. (2006) Creating a process-focused retention
schedule.
Info. Man. J.
40(5), 62-9.
Wise-Blackman, G.M. (2006) Out-of-specifi cation results
and the quality system approach to GMPs.
Pharma. Tech.
30, Supplement.
Woodrum, T. (2003) 21 CFR Part 11: The role of predicate
regulations and associated internal policies.
Drug Info. J.
37(2), 159-64.