Capture new insights into accelerating and streamlining processes at every stage of clinical research. Don’t miss this illuminating article from Certara. Read now for insights into:

Don’t miss insights from a recent recorded panel discussion among the subject matter area experts at Certara. Watch on demand to:

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Discover the importance of pre-submission validation, plus insights into accelerating the generation of define.xml files and Reviewer’s Guides. Watch now to explore:

Explore how Simcyp delivered benefits during multiple stages of the drug cycle, with these information-rich case studies from Certara. Read now for insights into:

Learn more about the purpose of EU-CTR and uncover best practices for adapting to its requirements, with insights from the experts at Certara. You will gain a deeper understanding of these regulations and the requirements of using its CTIS to submit, assess, authorize, supervise, and report on clinical trials in the EU. Read now to: