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Our Ask-the-Analyst service is your direct hotline to the team of experts who cover all aspects of the Pharmaceutical market including R&D, clinical trials, market access, financing and licensing. As a Medtrack subscriber, you will receive 24/7 access to our expert analysts who can answer your business development and licensing questions and will provide a
detailed response to your query, spending up to 3 hours per question they receive and will respond within 48 hours, subject to your terms and conditions.
The following examples are actual questions received from Medtrack subscribers, along with their sample responses from the Medtrack analyst team.
$name, Citeline Connect
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: The most widely used platform for clini...
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.
TrialScope Disclose: The most widely used platform for clini...
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.
Topics Clinical Trials
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