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Designing non-clinical safety evaluation programmes: The view of the clinician,1. Experience with biotechnologically derived pharmaceuticals to treat auto-immune diseases provides an example of the pharmacological and safety information pertinent to first entry into man, and the relevance of animal data in support of early clinical trials.AVOW 发表于 2025-3-25 07:35:04
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https://doi.org/10.1007/978-94-011-4876-4biotechnology; gene therapy; growth factor; interferon; research