Approach to maintaining comparability of biochemical data during long-term clinical trials.

Cull, CA; Manley, SE; Stratton, IM; Neil, HA; Ross, IS; Holman, RR; Turner, RC; Matthews, DR

Abstract:

Our objective was to design a structured approach to maintaining comparability of biochemical data during a long clinical trial. Maintaining the comparability of clinical and biochemical data obtained in long-term studies is essential, even though analytical methods in the laboratory may be changed, conventions on specimen handling and storage revised, calibration procedures updated, quality-control systems replaced, and secular changes may occur. The United Kingdom Prospective Diabetes Study...

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Published

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APA Style

Cull, C. A., Manley, S. E., Stratton, I. M., Neil, H. A., Ross, I. S., Holman, R. R., Turner, R. C., & Matthews, D. R. (1997). Approach to maintaining comparability of biochemical data during long-term clinical trials. Clinical Chemistry, 43(10), 1913–1918.

MLA Style

Cull, C. A., et al. “Approach to Maintaining Comparability of Biochemical Data during Long-Term Clinical Trials.” Clinical Chemistry, vol. 43, no. 10, Clinical chemistry, 1997, pp. 1913–18.

Chicago Style

Cull, CA, SE Manley, IM Stratton, HA Neil, IS Ross, RR Holman, RC Turner, and DR Matthews. 1997. “Approach to Maintaining Comparability of Biochemical Data during Long-Term Clinical Trials.” Clinical Chemistry 43 (10): 1913–18.
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