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Points to consider regarding the use and implementation of virtual controls in nonclinical general toxicology studies
Xavier Palazzi1, Lennart T Anger2, Theresa Boulineau3
1Drug Safety Research and Development, Pfizer Inc, 445, Eastern Point Road, Groton CT, USA.
Abstract:
The replacement of a proportion of concurrent controls by virtual controls in nonclinical safety studies has gained traction over the last few years. This is supported by foundational work, encouraged by regulators, and aligned with societal expectations regarding the use of animals in research. This paper provides an overview of the points to consider for any institution on the verge of implementing this concept, with emphasis given on database creation, risks, and discipline-specific perspectives.
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