Citeline Engage: Supporting clinical trial pl...

Téléchargez votre livre blanc gratuit, « Compte à rebours du nouveau règlement européen sur les essais cliniques : à quoi s'attendre et comment se préparer »

22 Oct 2021

Des changements majeurs arrivent, impactant toutes les étapes des essais cliniques, y compris les essais nouveaux et en cours – êtes-vous prêt ? Sachez à quoi vous attendre et comment maintenir votre conformité en matière de divulgation lorsque le nouveau système d'information sur les essais cliniques (CTIS), créé par l'Agence européenne des médicaments (EMA), entrera en vigueur.

Topic business-strategies clinical-trials

Citeline Engage: Supporting clinical trial pl...

CTIS Best Practices Whitepaper

19 Oct 2021

Europe’s new Clinical Trial Information System (CTIS), created by the European Medicines Agency (EMA), is due to be implemented in January 2022. Find out what sponsors must do to ensure compliance with this far-reaching new regulatory requirement.

Topic clinical-trials

Trialtrove: 医療用医薬品の臨床試験情報データベース

Introduction to the China Clinical Trials Landscape with Andy Benson

15 Oct 2021

Deep dive into China’s clinical landscape to learn more about the startling growth in clinical research in our whitepaper from Dr Annie Siu, PhD, MBA, APAC - Content Director, Informa Pharma Intelligence and Andrew Benson, MSc - Senior Director, Trialtrove.

Topic business-strategies clinical-trials

Generics Bulletin: ジェネリック＆バイオシミラーニュース

India Biosimilars Landscape

12 Oct 2021

India leads the ways with the highest number of approved biosimilars.

Topic clinical-trials biosimilars

Citeline

China Clinical Trials Landscape

28 Sep 2021

In 2017, Informa Pharma Intelligence took a deep dive into the clinical trial landscape in China over the previous 10 years, in a whitepaper entitled “Is China the Dark Horse in Clinical Development?”. That analysis showed that the number of trial starts in China had been trending upwards year-on-year and suggested that China was on course to become a formidable player within the pharma industry on a global stage.

Topic clinical-trials

Citeline Engage: Supporting clinical trial pl...

Clinical Trial Information System (CTIS)

14 Sep 2021

Created by the European Medicines Agency (EMA). Stakeholders will use CTIS to: Submit and approve clinical trial applications (CTAs), Submit trial reports, results and notifications, Communicate centrally with the Member States Concerned (MSC) in the clinical trial

Topic Policy & Regulation Clinical Trials Clinical Trials Blog

Accelerate clinical trial cycle times by sele...

Minimizing Luck in Study Feasibility

29 Jul 2021

This informative whitepaper introduces you to best practices in study feasibility, which laid the groundwork for our new predictive analytic that is launching soon, Citeline Study Feasibility.  Our industry-leading technology will deliver advanced insight to improve your clinical trial decisions, fast-track enrollment and optimize cycle times – all with less effort.

Topic Clinical Trials

Citeline Connect

Patient Perspectives on Clinical Trial Participation Report

22 Jul 2021

Informa Pharma Intelligence partnered with Rare Patient Voice to measure the pulse of the public in relation to clinical trial participation post-COVID-19

Topic clinical-trials