In clinical trial design, don't guess at inclusion/exclusion criteria

Feasibility estimates don’t have to be a historic average. You don't have to guess whether your study’s inclusion/exclusion, con meds, or patient visit schedule will help or hinder patient recruitment.

Learn From “On-the-Ground” Principal Investigators:

• Inclusion/exclusion criteria: Are they appropriate, complete?
• Competing studies: Which ones will cause recruiting issues?
• Standard of care: What are the implications in their facility/geography?
• Informed consent: Is it appropriate, how will patients react?
• Endpoints: Are they appropriate, what are other alternatives?
• Visit schedule: How will patients react, is it burdensome for the site?

Utilize Smart, Digital Technologies

ISR utilizes digital focus group technology that allows Principal Investigators to comment on and make suggestions to study protocols. Benefits of this web-based, non-real time application include:

• Convenience: PIs can respond when it is convenient for them
• Geographic reach: Accommodates PIs from different locations
• Peer-based forum: PIs can view other responses and comment on them
• Probing: Moderators can ask follow-up questions
• Speed: Responses can be analyzed quickly
• Transparency: Observers from your company can watch the group in real-time
• Cost effective: No travel costs

To learn more about ISR's Investigator Forum services, contact us at info@ISRreports.com.