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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:

  1. Product type dictates study design and trial characteristics
  2. Time spent developing patient profile prior to trial start saves time later
  3. Regulatory requirements influence patient profile and need for monitoring
  4. Patient profile guides recruitment and potential retention issues
  5. Study protocol compliance ensures data quality
  6. Risk-based approach to monitoring applies systematic process that helps prevent or mitigate important and likely risks to data quality and participants
  7. Cloud-based eClinical platform addresses challenges with trial enrollment, compliance and retention

Download the eBook now: