Featured Articles

31. Centralizing Global Content Solutions For Medical Affairs 6/26/2023

    Take a look at common challenges associated with decentralized content development inconsistencies and how centralized content development can benefit your next clinical trial.

32. The C3 Summit: San Francisco Recap 6/26/2023

    Briefly explore the main takeaways from each session held at the C3 Summit in San Francisco, primarily focusing on challenges and insights presented throughout the discussions.

33. Overcoming 5 Challenges Of Implementing eClinical Technologies 6/26/2023

    Assess five common pitfalls trial teams face when incorporating new technology and identify potential solutions to mitigate the common risks.

34. Centralizing Content Solutions For Patient Engagement Teams 6/26/2023

    Explore challenges often associated with patient engagement in clinical trials and how centralizing global content could play a part in revamping strategy.

35. Unitary Patents & Their Impact On Life Sciences Companies 6/26/2023

    Learn about the ways Unitary Patents (UP) are working to simplify systems for patent protection in the EU, such as streamlining validation and translation requirements and making the process more cost-effective and less complex.

36. IMP Labeling: EU CTR Transition Considerations 6/26/2023

    Review current requirements as outlined by the EU Clinical Trial Regulation, supporting guidance, and three key considerations when planning IMP labeling activities for ongoing studies.

37. Hearing The Patient Voice Through Technology & eCOA 6/26/2023

    Discover the benefits of gathering patient data through electronic clinical outcome assessments and electronic patient-reported outcomes over paper versions.

38. Benefits Of Centralizing Global Content Solutions For Regulatory Teams 6/26/2023

    Learn how to prioritize technology frameworks to centralize and manage multiple submissions and help organizations stay aligned with the evolving regulatory landscape.

39. Assessing Readiness For EU CTR: 5 Points To Consider 6/26/2023

    To evaluate readiness for the EU Clinical Trials Regulation, utilize these five key points to better analyze an organization's readiness and highlight any necessary adjustments for effective compliance.

40. The Ultimate Clinical Trial Tracking Checklist 6/15/2023

    Ensure 360° clinical trial management support with a CTMS that aggregates and reports on these fields faster and more efficiently than spreadsheet trackers and legacy clinical trial data systems.