Study Design & Medical Writing
A trial can succeed or fail based on the integrity and consistency of the study protocol, including the chosen endpoints. CAP understands the importance of focused study design, and is acknowledged as an expert in crafting comprehensive and well-written protocols.
Our study design team has the experience required by our clients to effectively and expertly focus on the specific needs of the client and the trial itself. Through frequent communication and collaboration with our clients, our team works to understand all the intricacies of the project, including indication-specific measures that may escape a less oncology – or supportive care – focused CRO. With a focus on accuracy and consistency, our team will work to ensure the study protocol makes sense both scientifically and logistically, which is a benefit to all parties.
Our study design & medical writing services include:
- Informed consent forms
- Clinical study reports
- FDA briefing documents
- Investigator’s brochures
- Abstracts, posters and journal articles
- Executive summaries for efficacy or safety
- Patient narratives