chevron_left
Rx for References: Learn how EndNote can help your research thrive
Speakers
From regulatory submissions to research publications, life sciences professionals face mounting pressure to manage literature and full text efficiently and collaboratively—without risking errors, delays or compliance issues.
Watch this webinar to see how EndNote—trusted by the NIH, FDA, leading pharmaceutical companies and top research universities—helps you take control of your research workflow and eliminate inefficiencies.
In this session, you’ll learn how to:
- Save time by importing from PubMed and organizing libraries with ease.
- Cut costs with full-text access via EndNote Click—no more duplicate purchases.
- Collaborate confidently across teams and with CROs.
- Format citations and documents automatically with Cite While You Write.
- Leverage customizable features and automation tools tailored to pharma and medical workflows.
Whether you’re managing regulatory submissions, research publications or internal documentation, this webinar will equip you with the knowledge and tools to boost productivity, ensure accuracy and streamline your entire reference management process.
