Blog Series: How to Diminish the Challenges of Data Collection in Oncology Clinical Trials

Jackie Brusch

CRF Health's Oncology-Focused
eCOA Blog Series

We're excited to announce a 5-part blog series to help oncology clinical trial professionals overcome everyday data collection challenges.

Here's the 5 topics:

1. How to Resolve Site Challenges with Collecting Patient Data During Oncology Clinical Trials​ What challenges are sites facing? If you're a site, you already know.  But do you know how to overcome them?  Are you working toward a better solution?

 2. Reducing Patient Challenges of Data Collection During Oncology Clinical Trials​ Does your current method of collecting data really support the patient or their caregiver?

3.  Enabling Easier Adverse Event Reporting and Concomitant Medication Collection During Oncology Clinical Trials Are you able to tell the difference between symptoms and side effects of the trial drug versus medication that relieves pain or other symptoms of chemotherapy?

4. Simplifying Data Collection in Post-Progression Oncology Clinical Trials Can your subjects participate in a trial at home?

5.  Minimizing Regulatory Risks with ALCOA during Oncology Studies​  Is your study in danger of failing regulatory approval?

Want to talk to a CRF Health eCOA expert? Contact us!

About the Author

Jackie Brusch

Jackie Brusch is the Content Marketing Manager at CRF Health.

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Understanding the Benefits of eCOA in Oncology Clinical Trials
Understanding the Benefits of eCOA in Oncology Clinical Trials

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Minimizing Regulatory Risks with ALCOA during Oncology Studies
Minimizing Regulatory Risks with ALCOA during Oncology Studies