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Simultaneous Global New Drug Development - Multi-Regional Clinical Trials after ICH E17 (Hardcover)
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Simultaneous Global New Drug Development - Multi-Regional Clinical Trials after ICH E17 (Hardcover)
Series: Chapman & Hall/CRC Biostatistics Series
Expected to ship within 12 - 17 working days
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Global simultaneous development is becoming more necessary as the
cost of developing medical products continues to grow. The strategy
of using multiregional clinical trials (MRCTs) has become the
preferred method for developing new medicines. Implementing the
same protocol to include subjects from many geographical regions
around the world, MRCTs can speed up the patient enrolment, thus
resulting in quicker drug development and obtaining faster approval
of the drug globally. After the publication of the editors' first
volume on this topic, there have been new developments on MRCTs.
The International Council for Harmonisation (ICH) issued ICH E17, a
guideline document on MRCTs, in November 2017, laying out
principles on MRCTs. Beyond E17, new methodologies have been
developed as well. Simultaneous Global New Drug Development:
Multi-Regional Clinical Trials after ICH E17 collects chapters
providing interpretations of principles in ICH E17 and new ideas of
implementing MRCTs. Authors are from different regions, and from
academia and industry. In addition, in contrast to the first book,
new perspectives are brought to MRCT from regulatory agencies. This
book will be of particular interest to biostatisticians working in
late stage clinical development of medical products. It will also
be especially helpful for statisticians in regulatory agencies, and
medical research institutes. This book is comprehensive across the
MRCT topic spectrum, including Issues regarding ICH E17
Implementation MRCT Design and Analysis Methodologies Perspectives
from authorities in regulatory agencies, as well as statisticians
practicing in the medical product industry Many examples of
real-life applications based on actual MRCTs.
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