FEATURED ARTICLES

• Empowering Your Team For Successful Clinical Trial Management

  Speakers provide insight into how clinical teams can better manage their drug development studies and associated trial master files.

• A Step In The Right Direction: GCP E6(R3) ICH Harmonized Guidelines

  Take a deep dive into the pivotal enhancements within the GCP E6(R3) ICH Harmonized Guidelines that are expected to have a substantial influence on trial execution and documentation.

• GlobalLearn: Study Team Training

  Feel confident that your study team training practices are comprehensive and aligned with both regulatory and corporate mandates by watching this presentation by Trial Interactive's Product Manager, GlobalLearn, Marc Gracieux.

• Kickstart Your CTMS Strategy

  Utilize this comprehensive checklist as a guiding framework to formulate a robust high-level plan that encompasses CTMS requisites and outlines the necessary training and documentation.

• EU CTR: Focus On CT Transitions

  Watch as TransPerfect Life Sciences Executive Director Pierre-Frederic Omnes explores topics surrounding trial transitions and answers common questions regarding new European requirements.

• The Top 5 Skills For A Successful TMF Team

  Gain insight from Trial Interactive’s Director of Client Solutions Laurel-Ann Schrader who outlines the top five skills team members should prioritize for their professional development.

• Maximizing Value & Avoiding Failure During Dealmaking

  Gain invaluable wisdom that can be applied to life sciences dealmaking from AstraZeneca and Merck's remarkable panel of experts.

• 10 Prompts For Optimizing Clinical Trial Recruitment With ChatGPT

  Consider these 10 questions when interacting with ChatGPT about how to improve patient recruitment, engagement, and retention efforts in your next clinical trial.

• 7 Considerations For Improving The App Localization Process

  Gain valuable insights and enhance the efficiency of app localization processes to ensure a smooth and multilingual patient experience, while also complying with local regulations and privacy laws.

• Intelligent Automation For MDR & IVDR Content

  Learn how automation can help fulfill new MDR/IVDR requirements and optimize existing labeling and documentation operations while meeting compliance.

• Operational Considerations For EU Clinical Trial Readiness & Execution

  Gain a comprehensive understanding of the Clinical Trial Regulation (EU) 536/2014 (CTR), which has equipped stakeholders to navigate the altered regulatory landscape and prepare for conducting clinical trials in the EU/EEA.

• The Future Of eCOA & Wearable Devices

  Learn how by looking at the advantages of wearables and where they are headed in the future, manufacturers, providers, and researchers can better anticipate collaboration efforts to bridge the gaps in existing processes and maximize the potential of eCOA wearables in clinical research.