Free eBook:
Best Practices
to Drive Time and Cost Savings for Your Women’s Contraceptive Clinical Trial
In this paper, you'll learn about 7 best practices you can apply to a women’s contraceptive study to ensure better enrollment, compliance, and retention, saving your trial time and costs:
- Product type dictates study design and trial characteristics
- Time spent developing patient profile prior to trial start saves time later
- Regulatory requirements influence patient profile and need for monitoring
- Patient profile guides recruitment and potential retention issues
- Study protocol compliance ensures data quality
- Risk-based approach to monitoring applies systematic process that helps prevent or mitigate important and likely risks to data quality and participants
- Cloud-based eClinical platform addresses challenges with trial enrollment, compliance and retention
