可憎
发表于 2025-3-25 04:22:00
New Approaches to Developmental Toxicity Risk Assessment at the U.S. Environmental Protection Agencyd, but low level, exposure of large segments of the general population through the food, water or air. Such situations are in direct contrast to the health risks associated with pharmaceutical agents, where the exposure is direct and controlled and the benefits accrue to the exposed individual.
Cleave
发表于 2025-3-25 08:20:56
Conference proceedings 1992xtensive research.Risk assessment of prenatally-induced adverse health effectsis still a difficult task from both experimental data aswell asfrom observations in humans. In the contributions tothis book three majoraspects are dealt with:- Quantitative extrapolations of experimental datato the situat
BLANK
发表于 2025-3-25 12:30:42
Reproductive Toxicity Risk Assessment — Some Questionspersonal risks is to attempt to stimulate examination of what we do from a different angle. If my attempt fails it should at least demonstrate that risk is relative since the contributions of other participants will appear more erudite.
STEER
发表于 2025-3-25 16:09:26
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STYX
发表于 2025-3-25 22:25:05
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欺骗世家
发表于 2025-3-26 00:43:56
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Collision
发表于 2025-3-26 05:00:24
Risk Assessment for Pharmaceutical Productsreproductive toxicity in laboratory animals. Considerable progress has been made in improving the design of these studies, and draft guidelines have been promulgated which reduce the redundancy and increase the flexibility of reproductive toxicity tests for drug safety evaluation (Bass et al. 1991;
COLON
发表于 2025-3-26 08:45:58
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sacrum
发表于 2025-3-26 13:29:29
Biomarkers of Developmental Neurotoxicitycal or physical agent. Neurotoxic effects may be permanent or reversible, produced by neuropharmacological or neurodegenerative properties of a neurotoxicant, or the result of direct or indirect actions on the nervous system (ICON 1990). Adverse effects include: unwanted side effects, effects due to
初学者
发表于 2025-3-26 19:17:22
Assessment of Reproductive Toxicology of Drugs at the Food and Drug Administrationhe Food and Drug Administration is also interested in an internationally harmonized approach to evaluating reproductive and developmental toxicity. The evolving harmonization guideline, that contains input from many sources, is as flexible a document as possible. It addresses multiple approaches, ad