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Get in-depth and insightful information about the pharmaceutical and medtech industries with pharmaceutical whitepapers from Pharma Intelligence. Covering a range of topics and specialty areas, these informative and authoritative whitepapers present insights and information not found elsewhere.
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TrialScope Atlas
19 May 2022
Clinical trial disclosure is a complex process driven by a constantly evolving collection of registry rules and health authority regulations.
Topic Regulation
Topic Clinical Trials
Citeline, Pharmaprojects
By Ian Lloyd 14 Apr 2022
Our world was disrupted at warp speed during 2020. Are you ready to gain a deeper understanding of the year that changed our perceptions of possible?
TrialScope Disclose
07 Feb 2022
Disclosure requirements are numerous and ever evolving. Study sponsors need a transparency policy that addresses disclosure, transparency, and data sharing.
Topic Policy & Regulation
Citeline
02 Feb 2022
In our rare disease trial strategies whitepaper, see which sponsors lead the way, understand the geographical location of trials, and delve into the types of therapeutic area, plus much more.
Topic Rare Diseases
TrialScope Disclose
11 Jan 2022
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.
Citeline Connect
06 Dec 2021
Accelerate study startup, drive engagement, and enable community and communication surrounding your clinical trials with Citeline Connect, the only end-to-end platform supporting all aspects of clinical trial recruitment.
TrialScope Disclose
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
18 Oct 2021
本白皮书由Annie Siu博士（PhD，MBA，亚太地区Informa Pharma Intelligence内容总监）与Andrew Benson（MSc，Trialtrove高级总监）撰写，深入剖析中国临床试验的整体格局，介绍临床研究取得的惊人发展。
Topic China
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