转折点
发表于 2025-3-27 00:13:07
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custody
发表于 2025-3-27 02:26:13
Hexamethylenetetramine (Hexamine),role of computers. Computers have transformed drug discovery form hit-and-trial approach to rational drug design. Initial quantitative structure-activity relationship (QSAR) studies led to the foundation of computer-aided drug design (CADD), which subsequently evolved to structure-based drug design
Mangle
发表于 2025-3-27 07:36:48
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FLACK
发表于 2025-3-27 11:35:07
Ethanolamines and Secondary Products,now being transformed to the concept of ‘Quality by Design’ (QbD) with the adoption of QbD by most of the drug regulatory agencies across the globe. QbD ensures systematic adoption of certain approaches, such as DoE, risk assessment, and process analytical technology, for the development of pharmace
被诅咒的人
发表于 2025-3-27 17:29:14
Ammonium Phosphates and Ammonium Sulfate,d followed for years is not only expensive and time-consuming but also needs a lot of efforts in spite of which they are unfavorable and unpredictable at times. “Pharmaceutical Quality by Design” (QbD) is a well-organized approach which focuses an attention on product, process understanding, and pro
Engaging
发表于 2025-3-27 20:03:58
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MEEK
发表于 2025-3-27 23:05:41
Ethanolamines and Secondary Products,gn (CAD) and allows machines to build artefacts directly from the fed designs into the software without any manual intervention to set up machines and processes. CAM machines can manufacture thousands of similar products automatically in very little time. As conventional pharmaceutical manufacturing
Schlemms-Canal
发表于 2025-3-28 04:50:09
Ethylenediamine and Chelating Agents,le in formulating an efficient dosage form with appropriate bioavailability. Absorption of drugs is a multifaceted process affected by several factors including the physicochemical properties of the drug and the pharmaco-technical parameters of the formulation. Several drugs during their development
hardheaded
发表于 2025-3-28 07:13:02
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Anthem
发表于 2025-3-28 12:23:18
Hexamethylenetetramine (Hexamine),egral part of drug discovery and development process, it has also gained worldwide acceptance by drug regulatory bodies. PBPK models correlate drug properties with information of the physiology and biology of a species, in order to achieve a mechanistic representation of the drug in biological syste