Resources and Templates
Access our curated collection of templates and guides designed for clinical research professionals. Find practical resources that ensure regulatory compliance and support patient-centered trial design.
In-trial interviews request for proposal (RFP) template
In collaboration with our clients, we've created an RFP template to make it easier to formulate requests for in-trial interview proposals, while ensuring you meet all regulatory requirements and fulfill the essential standards for conducting interviews in clinical trials.
Cognitive debriefs:
an essential guide
What if patients interpret your questions differently than you intended? Cognitive debriefs uncover interpretation gaps and ensure your COAs work for your target population. Investment in a cognitive debrief study can prevent costly data errors.
Concept elicitation:
an essential guide
The investment in high-quality concept elicitation studies can pay dividends throughout the drug development process, from early endpoint selection through regulatory approval and post-market evaluation of therapeutic benefit.
Understanding patient-centered research
Anna Ryden (PhD), Chief Scientific Officer, explains how in-depth qualitative interviews capture the patient experience in drug development.
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