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Shorten Start-Up Timelines in Vaccine Trials
Six Factors Critical to Success
Speed is crucial in clinical development, especially for infectious disease vaccine trials. Factors like competition and global health crises make time-to-market vital. The COVID pandemic has set a new standard for vaccine development, with some trials completing in under a year. Prioritization and special waivers helped achieve this speed, resetting expectations. We believe that six areas are most significant in impacting the efficiency of the study start-up phase:
Download our ebook to gain insights and strategy in how to:
- Leverage local expertise to avoid delays
- Engage key personnel early to ensure alignment
- Navigate regulatory and ethical approvals efficiently
- Develop and implement a robust operational plan
- Develop effective recruitment strategies
- Harness technology to accelerate building the trial database