chungcho - 電子書籍 1

「メガアウトブレイク」によりオーガの襲撃が始まる！ドヒョクはオーガロード・イベナールとの壮絶な戦いを始める。そのかたわら、韓国のギルドたちの間でも戦争が勃発する。 一方、仲間だったソンミとの間では恋……続きを見る

ゲーム「D&F」と現実とのつながりは本物だった。ドヒョクはダンジョンから、D&Fの登場人物である「ヘイズ」という女性を救出してきたのである。 そして、本格的に「D&F」の世界とストーリーを知るべく、ストーリー……続きを見る

平凡なネトゲ廃人だったパク・ドヒョクはある日、世界唯一の「呪文使い」として覚醒した。しかもごく稀な「トリプル覚醒者」。 それ以来、彼は超巨額の契約金をもらってギルドと傭兵契約を結び、女性タンカーのマ……続きを見る

「Ｄ＆Ｆでの能力を、現実で使えれば楽しいだろうな」 大好きだったゲームのサービス終了日に言った途方もない願いが現実になった。「Ｄ＆Ｆ」の能力を持つ「呪文使い」として覚醒したのだ！ 平凡なネトゲ廃人だっ……続きを見る

ゲーム「D&F」での能力で覚醒した呪文使い、パク・ドヒョク。 しかしダンジョンの攻略中、彼は「D&F」の登場人物だったキャラクターと出会い、思いもよらぬ力を手に入れる。 さらにアメリカに渡って入ったダンジョ……続きを見る

In clinical trial practice, controversial statistical issues inevitably occur regardless of the compliance with good statistical practice and good clinical practice. But by identifying the causes of……続きを見る

Preeminent Experts Update a Well-Respected BookTaking into account the regulatory and scientific developments that have occurred since the second edition, Design and Analysis of Bioavailability and ……続きを見る

Praise for the Second Edition: "… this is a useful, comprehensive compendium of almost every possible sample size formula. The strong organization and carefully defined formulae will aid any researc……続きを見る

As many biological products face losing their patents in the next decade, the pharmaceutical industry needs an abbreviated regulatory pathway for approval of biosimilar drug products, which are cost……続きを見る

The US Food and Drug Administration's Report to the Nation in 2004 and 2005 indicated that one of the top reasons for drug recall was that stability data did not support existing expiration dates. P……続きを見る

"Offers a comprehensive, unified presentation of statistical designs and methods of analysis for all stages of pharmaceutical development--emphasizing biopharmaceutical applications and demonstratin……続きを見る

Emphasizing the role of good statistical practices (GSP) in drug research and formulation, this book outlines important statistics applications for each stage of pharmaceutical development to ensure……続きを見る

With new statistical and scientific issues arising in adaptive clinical trial design, including the U.S. FDA's recent draft guidance, a new edition of one of the first books on the topic is needed. ……続きを見る

In the United States, a rare disease is defined by the Orphan Drug Act as a disorder or condition that affects fewer than 200,000 persons. For the approval of "orphan" drug products for rare disease……続きを見る

Statistical methods that are commonly used in the review and approval process of regulatory submissions are usually referred to as statistics in regulatory science or regulatory statistics. In a bro……続きを見る

First published in 1989. This is a collection of essays, excerpts of Korean classical literature including areas of romance, and selected work of Park Jiwon. Samsolgi is a collection of nine allegor……続きを見る

In recent years, many pharmaceutical companies and clinical research organizations have been focusing on the development of traditional Chinese (herbal) medicines (TCMs) as alternatives to treating ……続きを見る

This work details the statistical inference of linear models including parameter estimation, hypothesis testing, confidence intervals, and prediction. The authors discuss the application of statisti……続きを見る

This book focuses on analytical similarity assessment in biosimilar product development following the FDA’s recommended stepwise approach for obtaining totality-of-the-evidence for approval of biosi……続きを見る

Provides a comprehensive review of all types of medical therapeutic delivery solutions from traditional pharmaceutical therapy development to innovative medical device therapy treatment to the recen……続きを見る

Praise for the Second Edition: “...a grand feast for biostatisticians. It stands ready to satisfy the appetite of any pharmaceutical scientist with a respectable statistical appetite.” ーJournal of ……続きを見る