Ditemukan 13 dokumen yang sesuai dengan query
The pace of therapeutic advances in the treatment of cardiovascular diseases is rapid, and new clinically–relevant information appears with such frequency that it can be extremely challenging for clinicians to keep up. Still, knowledge and interpretation of major clinical trials is crucial for the range of clinicians who manage cardiovascular...
Chichester, West Sussex, U.K.: Blackwell , 2013
e20375781
eBooks Universitas Indonesia Library
This book will examine current issues and controversies in the design of clinical trials, including topics in adaptive and sequential designs, the design of correlative genomic studies, the design of studies in which missing data is anticipated. Each chapter will be written by an expert conducting research in the...
New York: Springer, 2012
e20417633
eBooks Universitas Indonesia Library
M. Sopiyudin Dahlan, examiner
Jakarta: Sagung Seto, 2021
617.02 SOP m
Buku Teks Universitas Indonesia Library
Selene Baschieri, editor
The aim of this book is to provide an overview of some of the technology platforms that have been realized or are currently under development to try to address unsolved and new issues in the field of vaccine development...
Dordrecht: [, Springer], 2012
e20417325
eBooks Universitas Indonesia Library
Ton J. Cleophas, author
In the past few years the authors of this 5th edition, as teachers and research supervisors in academic and top-clinical facilities, have been able to closely observe the latest developments in the field of clinical data analysis, and they have been able to assess their performance. The novel methods are...
Dordrecht: [, Springer], 2012
e20417558
eBooks Universitas Indonesia Library
Brody, Tom, author
Amsterdam: Elsevier/Academic Press, 2012
615.507 24 BRO c
Buku Teks Universitas Indonesia Library
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...
Hoboken, New Jersey: John Wiley & Sons, 2010
e20376693
eBooks Universitas Indonesia Library
Kazmierski, Wieslaw M., editor
This book focuses on new small molecule approaches to combat viral infections. The chapters describe the discovery and development from bench through the clinic of relatively recently-approved antiviral drugs and compounds in advanced clinical development. Organized by a virus (such as HIV, HCV, RSV, influenza, HBV and CMV) and written...
New Jersey: John Wiley & Sons, 2011
e20375714
eBooks Universitas Indonesia Library
This book discusses key statistical concepts that facilitate the inferential analysis of data collected from a group of individuals participating in a pharmaceutical clinical trial, the estimation of their clinical significance in the general population of individuals likely to be prescribed the drug if approved, and the related decision-making that...
New York: Springer, 2012
e20401564
eBooks Universitas Indonesia Library
Cleophas, Ton J., author
The first part of this title contained all statistical tests relevant to starting clinical investigations, and included tests for continuous and binary data, power, sample size, multiple testing, variability, confounding, interaction, and reliability. The current part 2 of this title reviews methods for handling missing data, manipulated data, multiple confounders,...
Dordrecht: [Springer, ], 2012
e20419546
eBooks Universitas Indonesia Library
