In this webinar, the expert speakers guide the audience through key strategies for overcoming the most common hurdles encountered in early-phase clinical trials. They provide insights into optimizing trial design for scalability, selecting technology solutions that support long-term growth and ensuring high standards of data quality across all phases.
Gain an understanding of:
- How a robust approach to data management not only helps meet regulatory requirements but also improves operational efficiency, accelerates timelines and strengthens the case for payer reimbursement.
- Practical aspects of early-phase trial management, including common pitfalls that can delay or derail progress and how to proactively address them.
- Real-world examples of companies that have successfully navigated these early stages, including strategies they employed to achieve regulatory milestones and prepare for future trial phases.
- How to choose the right CDMS/EDC features to support evolving needs and maintain data integrity, thus emphasizing the importance of adaptability in clinical research.
Speakers
- Bryan Terry, Senior Data Manager, Inozyme Pharma
- Kate Smith, MPH, Vice President, Clinical Affairs, Lumicell
- Nicole Latimer, Chief Executive Officer, Medrio