Ditemukan 12 dokumen yang sesuai dengan query
Oxford: Blackwell, 1977
615.19 CLI
Buku Teks Universitas Indonesia Library
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Drug Safety Evaluation has been written with the central objective of presenting an all-inclusive practical guide for those who are responsible for ensuring the safety of drugs and biologics to patients, health care providers, those involved in the manufacture of medicinal products, and all those who need to understand how the safety of these products is evaluated ...
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New York: John Wiley & Sons, 2002
e20385348
eBooks Universitas Indonesia Library
Harahap, Yahdiana
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Rebamipid tergolong suatu obat antiulkus yang masuk dalam kategori obat wajib uji Bioekivalensi (BE) menurut Food and Drug Administration (FDA). Penelitian ini bertujuan untuk memperoleh kondisi optimum untuk analisis rebamipid dalam plasma in vitro menggunakan Kromatografi Cair Kinerja Tinggi (KCKT) detektor ultraviolet dan melakukan validasi metode analisis tersebut. Kromatografi dilaksanakan dengan teknik isokratik pada kolom fase terbalik Kromasil® C18 (5 μm, Akzo Nobel) panjang kolom 250 x 4,6 mm, fase gerak asetonitril-dapar fosfat pH 3,0 ...
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Depok: Fakultas Farmasi Universitas Indonesia, 2009
AJ-Pdf
Artikel Jurnal Universitas Indonesia Library
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This book covers the methods and applications of bioassays in pharmaceutical science to quantify drug activity and evaluate the validity of models. It demonstrates the numerous systems available and that each system interprets the activity of drug molecules in different ways. The authors discuss the various models put forward to link the experimental observations and the events taking place on a cell or molecular level between the drug and experimental object, providing the principal and ...
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Hoboken, New Jersey: John Wiley & Sons, 2009
e20394488
eBooks Universitas Indonesia Library
Song, Seo Woo
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This thesis demonstrates a technology that enables pipetting-free high-throughput screening (HTS) on a miniaturized platform, eliminating the need for thousands of one-by-one pipetting and conventional liquid handling systems. This platform enhances accessibility to HTS and enables HTS to be used in small-to-medium scale laboratories. In addition, it allows large-scale combinatorial screening with a small number of valuable cells, such as patients primary cancer cells. This technique will have a high impact for widespread use of ...
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Singapore: Springer Nature, 2019
e20509327
eBooks Universitas Indonesia Library
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"This book presents a structural approach to the evaluation of herbal medicinal products for quality, safety and efficacy. There has been an enormous growth in the market for herbal medicinal products in the last twenty five years. However the rediscovery of natural substances with therapeutic potential has raised questions of quality, safety and efficacy on the part of the consumer and also from health professionals. This book brings together current thinking and practice in these ...
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London: Pharmaceutical Press, 2009
615.321 EVA
Buku Teks Universitas Indonesia Library
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All clinical investigators, sponsors, and Institutional Review Boards have to comply with the applicable FDA code(s). Good Clinical Practice (GCP) Audit Preparation provides a step-by-step explanation of the FDA audit procedures for clinical trials and how a pharmaceutical company should prepare for regulatory audits. The book emphasizes the processes and procedures that should be implemented before a clinical audit occurs, making this an imperative guide to any professional in the drug manufacturing industry, including drug ...
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Hoboken, New Jersey: John Wiley & Sons, 2010
e20376693
eBooks Universitas Indonesia Library
Chang, Mark
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ExpDesign Studio facilitates more efficient clinical trial design. This book introduces pharmaceutical statisticians, scientists, researchers, and others to ExpDesign Studio software for classical and adaptive designs of clinical trials. It includes the Professional Version 5.0 of ExpDesign Studio software that frees pharmaceutical professionals to focus on drug development and related challenges while the software handles the essential calculations and computations. After a hands-on introduction to the software and an overview of clinical trial designs encompassing ...
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Hoboken, New Jersey: John Wiley & Sons, 2008
e20376690
eBooks Universitas Indonesia Library
Tsaioun, Katya, editor
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This book guides medicinal chemists in how to implement early ADMET testing in their workflow in order to improve both the speed and efficiency of their efforts. Although many pharmaceutical companies have dedicated groups directly interfacing with drug discovery, the scientific principles and strategies are practiced in a variety of different ways. This book answers the need to regularize the drug discovery interface; it defines and reviews the field of ADME for medicinal chemists. In ...
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New Jersey: John Wiley & Sons, 2011
e20375655
eBooks Universitas Indonesia Library
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This book covers both recent advances in the design and synthesis of new drugs, as well as the myriad other issues facing a new drug candidate as it moves through the development process. Utilizing recent case studies, the authors provide valuable insights into the complexities of the process, from designing new synthetic methodologies and applying new automated techniques for finding optimal reaction conditions to selecting the final drug form and formulation ...
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Hoboken, New Jersey: Wiley-Interscience, 2006
e20395907
eBooks Universitas Indonesia Library
