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What is Citeline?

Clinical R and D

Citeline is the industry’s most comprehensive, reliable and current global R&D intelligence suite of solutions. Built by experts, made for experts, Citeline solutions transform data into knowledge. And now our new, next generation platform delivers unparalleled access to Citeline’s robust clinical trial intelligence. With greater ease, speed and efficiency than ever before, Citeline’s next generation platform will help you gain critical insights into the global clinical trial landscape and realize greater cost-savings as you develop on your clinical trial programs.

What Citeline does: 

Citeline organizes vast quantities of data with human intelligence to greatly reduce research time, clinical trial costs and optimize trial outcomes. It features an unmatched collection of critical information on global clinical trials, investigators and sites, and drug development pipelines all with direct expert analyst support. Stay updated on what your competitors are doing with full public domain coverage of over 40,000 sources, continuous updating and full record reviews, advanced indexing and proprietary content.

Gain key insights that can be turned into actionable results with unparalleled access to 265,000+ clinical trials, 400,000 investigators, 68,000+ drugs, 117,000+ sites, 235+ diseases in 8 major therapeutic areas across 166 countries. And our 250+ therapeutic area experts and analysts are dedicated to provide the support needed so that you’re getting the most appropriate data to meet your requirements.

Citeline solutions:

 

If you are a Citeline subscriber, please access your login here.

Related products

sitetrove-pharmaintelligence

Sitetrove: 治験責任医師と治験施設情報のデータベース

Sitetrove(サイトトローブ)は、170か国・40万人以上の治験責任医師(PI: Principal Investigator)と235以上の疾患に対応する11万7千か所以上の治験施設に関する情報を収録するデータベースです。治験責任医師と治験施設に関して業界で最も正確で包括的な情報を提供することで、コスト増につながる治験の遅延を最小化し、お客様の臨床試験を成功に導くようサポートします。Sitetroveに登録される治験責任医師は、豊富な臨床経験や治験に関する十分な知識をもっていることをアナリストにより精査されています。

Key benefits:

  • 治験責任医師と治験施設情報のデータベース
  • 疫学ダッシュボードは見やすいマップビュー
  • Ask-the-Analyst機能で情報に基づく意思決定
trial-trove-pharma intelligence

Trialtrove: 医療用医薬品の臨床試験情報データベース

Trialtrove(トライアルトローブ)は医療用医薬品の開発状況を常に把握できる医薬品業界随一の臨床試験情報データベースです。計画段階から完了まで、260疾患・29万件の臨床試験をトラッキングし、250以上の学会をカバーしています。4万以上の情報ソースから収録した臨床試験に関するデータを250名のアナリストが精査し、リアルタイムで更新しています。学会発表や企業発のニュースは即日収録されます。アラート機能や可視化ツールを活用することで、特定の臨床試験のモニタリングや資料作成も可能です。

Key benefits:

  • 専門家による情報精査
  • 世界中の臨床試験情報を網羅
  • 標準治療に関する情報
pharma intelligence pharma banner

Pharmaprojects: 医薬品開発パイプラインのデータベース

Pharmaprojects(ファーマプロジェクツ)は、医薬品業界で代表的な開発パイプライン(医療用医薬品候補化合物)のデータベースとして、医薬品企業をはじめとする多くのお客様にご利用いただいています。前臨床試験から上市済み医薬品まで、現在開発中の15,000の薬剤を含む68,000以上の開発パイプライン情報を収録しています。さらに、43,000以上の医薬品を網羅した35年間にわたる過去のデータベースにもアクセスできます。グローバル競争が激しくなる中、競合分析や研究開発戦略の策定に威力を発揮するデータベースです。

Key benefits:

  • 医療用医薬品の研究・開発パイプライン情報
  • 35年間にわたる過去のヒストリカルデータも
  • Ask-the-Analyst機能で情報に基づく意思決定
Citeline analytics

Citeline Analytics

Citeline’s Custom Analytics service provides expert analytical and project-orientated support for your strategic business questions.

Key benefits:

  • Actionable intelligence
  • Expert Analysis
  • Tailored solutions

無料の最新記事&レポート

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    The effect of COVID-19 on clinical trials, the industry response, and the return to full operations

    Topic Coronavirus clinical-trials

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    Topic Coronavirus FDA Drug Review

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  • Biomedtracker: 開発中医薬品をFDA承認確率で評価

    A Historic Decade of Deal Making

    A Historic Decade of Deal Making

    In preparation for the webinar, download your free infographic, a snapshot view of M&A’s biggest deals and major players and what their activities indicate for the year ahead.

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    COVID-19 Infographic

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    Access the infographic below which explores the number of treatment drugs for COVID-19 currently in clinical trials or in development, events including progress updates, partnerships, regulatory and trial announcements etc, and the number of articles published on COVID-19 as of March 3, 2020. This data has been tracked and reported via Informa Pharma Intelligence’s clinical, regulatory and commercial data and analytics, and news and insight tools including Biomedtracker, Trialtrove, Pharmaprojects, Scrip, Pink Sheet, Medtech Insight, and Generics Bulletin etc.

    Topic Coronavirus

  • Biomedtracker: 開発中医薬品をFDA承認確率で評価

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    2020 Early Outlook Webinar

    Anticipate the biggest, most impactful expected catalysts of early 2020 with the guidance and insights from Pharma Intelligence. Building off Biomedtracker’s Early 2020 Outlook report, our live webinar will include market context for these upcoming milestones and additional insights from Datamonitor Healthcare’s Therapeutic Area Directors.

    Topic fda

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    38th Annual J.P. Morgan Healthcare Conference Review

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    2019 Post-ASH Conference Report Extract

    Access vital post-ASH meeting reporting from the expert analysts at Datamonitor Healthcare and Biomedtracker.

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    2019 Post-ESMO Conference Report Extract

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    Topic Cancer Drug development landscape Research

  • Biomedtracker: 開発中医薬品をFDA承認確率で評価

    Major Mergers & Acquisitions Highlights from Q1 2019

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    Topic Business strategies Company analysis

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    Q4 2019 Outlook Report Extract

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    What major drug catalysts and events can you expect to see this quarter? Get a view of what's to come with an extract from the full report.

    Topic clinical-trials drug-development-landscape

  • Biomedtracker: 開発中医薬品をFDA承認確率で評価

    Q3 2019 Catalyst Roundup

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    Topic Drug approval Drug review FDA

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    Topic drug-approval drug-review drug-development-landscape

医薬品産業専門のジャーナリスト&アナリスト

Management

Susan Danheiser

Management, Director

Boston, USA

Susan Danheiser

Susan specializes in

  • Commercial Strategy
  • Clinical Trials
  • Oncology
  • Neurology

+24 year(s) experience

製品説明を兼ねた無料デモ&お問い合わせ

専任スタッフによる詳しい説明を兼ねた無料デモンストレーションを常時受け付けています。ご希望の場合は下記のフォームよりお気軽にお申し込みください。

ご質問等ございましたらお気軽にご連絡下さい。

日本(平日:9時~18時)
電話:+81 (0)3 6273 4260
Email:inquiry.jp@informa.com

オンラインショップのレポートストアでは、医療用医薬品の市場調査・分析レポートを常時1000本以上販売しています。レポート1本単位で購入でき、オンラインでご提供いたします。

お探しの情報が見つからない場合はお問い合わせ先までお気軽にご連絡ください。