Featured Articles

  1. The eTMF As A Regulatory Standard 6/1/2023

    Discover essential insights on maintaining a high-quality Trial Master File (TMF) in a discussion about ICH GCP Essential Documents and the different regulations that apply to the TMF.

  2. The Race To Implement A Connected eTMF-CTMS 5/25/2023

    Sponsors and CROs are becoming more dependent on CTMS-eTMF integration. Watch as experts examine the operational, regulatory, and financial advantages of this integrated technology.

  3. Virtual Investigator Meetings: The New Normal 5/23/2023

    Explore the benefits, challenges, and innovative solutions that make remote collaboration and engagement a vital part of successful research and development in the life sciences industry.

  4. Maximizing Efficiency And Compliance In Clinical Trial Site Training 5/16/2023

    Maintaining protocol adherence is essential to carrying out successful clinical trials. Learn how to streamline processes and enhance performance to drive success in drug development studies.

  5. CTMS & Study Data: 2 Keys To Creating Optimal Process Transparency 5/8/2023

    Clinical trial management systems can either make or break operational workflows in medical studies. Listen to this discussion with Hope Weisser, Sr. Product Manager at TransPerfect, about the new features of Trial Interactive’s CTMS.

  6. Professional Annotation For Better AI In Life Sciences 3/29/2023

    Discover how the industry has begun leveraging the full potential of its data reserves with the help of artificial intelligence and machine learning.

  7. Essential Documents vs. Expected Documents vs. Required Documents 1/24/2023

    What's the difference between Essential documents, Expected documents, and Required documents? Find out more in this blog about how to achieve TMF completeness.

  8. Children Are Not Just Small Adults: Considerations For Improving The Pediatric Experience 12/16/2022

    Delve into the challenges in rare disease and how they are only heightened for younger patient populations, where outcome measures and dosages need to be considered appropriately.

  9. Investigational Medicinal Products: Labeling Changes And Their Implications 12/16/2022

    Learn about Annex VI, which covers changes in the labeling requirements for investigational medicinal products (IMPs) and harmonizes them throughout EU countries.

  10. 3 Automation Outcomes For Pharmacovigilance And Safety Teams 12/14/2022

    With the continued implementation of AI and automated systems into the clinical process, learn how automated data management systems have helped to alleviate manual burdens on safety teams.