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Titlebook: Drug Discovery and Development; From Targets and Mol Ramarao Poduri Book 2021 Springer Nature Singapore Pte Ltd. 2021 Drug discovery.Pharma

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樓主: Covenant
41#
發(fā)表于 2025-3-28 16:44:24 | 只看該作者
Historical Perspective of Drug Discovery and Development,iscovery and development. The regulatory processes became stringent due to some adverse events in the second half of the twentieth century. Currently the digital and disruptive technologies are changing the scenario of drug discovery and development and producing efficacious and safe drugs.
42#
發(fā)表于 2025-3-28 20:39:10 | 只看該作者
Dynamic Axial Chirality in Drug Design and Discovery: Introduction to Atropisomerism, Classificatio relevant examples of drugs both from synthetic and natural origin. The chapter further extends to deal with various methodologies involved in atropselective conversions and regulatory guidelines involved in the development of atropisomers.
43#
發(fā)表于 2025-3-28 23:33:48 | 只看該作者
Regulatory Toxicology Testing of Pharmaceuticals,onclinical toxicology testing. To harmonize and avoid duplication of toxicological testing on animals to get approval for marketing across the globe, ICH issued unified guidelines. The different toxicological tests which are required for the new drug approval are briefly reviewed.
44#
發(fā)表于 2025-3-29 03:41:32 | 只看該作者
Pharmacovigilance,tudents to begin understanding the subject. It covers the drug safety frameworks and definitions of terms most commonly used in pharmacovigilance. Emphasis is laid on the methods used for characterization of adverse drug reactions.
45#
發(fā)表于 2025-3-29 10:36:05 | 只看該作者
46#
發(fā)表于 2025-3-29 13:46:11 | 只看該作者
Book 2021ncept of receptor interactions with regard to the initial stages of drug discovery. In a single, highly readable volume, it outlines the basics of pharmacological screening, drug target identification, and genetics involved in early drug discovery.?The final chapters introduce readers to stem therap
47#
發(fā)表于 2025-3-29 15:59:48 | 只看該作者
Regulatory Process for New Drug Approval in India,ective to treat the human diseases. Prior to clinical trials in humans, the drug must have desired pharmacological activity and no toxic effects in animals. The experimental protocols to be followed need to be approved by the Ethics Committee for trial to be registered. Clinical studies are generally carried out in four stages/Phases.
48#
發(fā)表于 2025-3-29 21:32:47 | 只看該作者
Richard Satherley,Mark W. Jonesiscovery and development. The regulatory processes became stringent due to some adverse events in the second half of the twentieth century. Currently the digital and disruptive technologies are changing the scenario of drug discovery and development and producing efficacious and safe drugs.
49#
發(fā)表于 2025-3-30 02:35:26 | 只看該作者
50#
發(fā)表于 2025-3-30 06:22:26 | 只看該作者
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