Project Management for
Patient Interview Studies

Our dedicated project managers seamlessly integrate in-trial patient interviews and real-world evidence into your complex studies, delivering ICH-GCP compliant data on time and within budget. Partner with CLINIGMA^® for efficient, high-quality patient data collection, anywhere in the world.

Seamless in-trial interview coordination

We make in-trial interviews simple for sponsors, clinical sites, and patients. We understand the complexities of conducting in-trial interviews and the difficulties this can bring when not executed correctly. Our expert team guides you through every step of the process.

Our solutions-based ethos to project management is key to delivering high quality ICH-GCP compliant interview services. Supported by our rigorous protocols, quality management system, and the CLINIGMA^® Portal, our dedicated team tailors solutions to the unique requirements of every project.

Seamless implementation

We understand how to overcome obstacles to make in-trial interviews easy for clients, clinical staff, interviewers, and patients. We adapt our approach to the unique requirements of your project while maintaining compliance with ICH-GCP and other regulations.

Meticulous planning

Our years of experience mean we can plan every aspect of your project in detail and adapt to changes or challenges quickly. Comprehensive plans are used for proactive risk management, safety reporting processes, and quality assurance, providing a structured framework to maintain timelines and budgets.

Open communication

We value open, transparent communication with clients and across every team involved in your study—to deliver high-quality services and client satisfaction. We share good news and challenges to identify issues early and proactively solve problems in partnership with you.

Transparent practices

Every aspect of the project is documented and agreed upon, providing clarity to support informed decision-making. Audit trails create a complete, chronological record of all activities, decisions, and communication.

Aligned with stakeholders

We listen and align with your needs. We help ensure all internal and external experts and stakeholders are included to optimize your interview study for regulatory submission and commercial decision-making.

Determined to succeed

We are here to help you succeed. Our project managers are approachable, available, and responsive to your needs. We share your commitment to include patient voices in drug development.

Expert execution & compliance

We navigate the complexities of in-trial interviews as a trusted and experienced partner in compliance with ICH-GCP, local laws, and regulatory standards for the submission of patient experience data.

Compliance

Regulatory alignment with FDA, EMA, and other regulatory agencies.

Quality assurance

For excellence in service delivery, data security, and patient safety.

Making in-trial patient interviews easy

CLINIGMA^® makes in-trial interviews simple and hassle-free while ensuring ICH-GCP compliance. We partner with you and use our expertise to overcome the challenges unique to each project.

Client Testimonials

I think you guys are amazing. We need more vendors like this! We are very, very satisfied with CLINIGMA^®. If I had to do an interview sub-study again, I would definitely push to do it with CLINIGMA^®.

Why our team makes the difference

One of the things I LOVE and appreciate about CLINIGMA^® is the people. CLINIGMA^®'s supportive culture and commitment to help clients achieve their goals is undoubtedly one of our key strengths. Our solution-focused ethos helps us develop as an organization—to deliver exceptional results for our clients.

Elisabeth Clasen

Senior Project Manager

For seamless in-trial interviews

CLINIGMA^® is a market leader for ICH-GCP compliant in-trial interviews. We are a dedicated team of experts, delivering high quality services. Find out how we can help you.