Project Management
Our dedicated project managers seamlessly integrate patient interviews 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.
Making in-trial interviews easy
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 guide you through every step of the process. Our solutions-based ethos to project management is key to delivering highality ICH-GCP compliant interview services. Supported by our rigorous protocols, QMS, 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 and quality assurance, providing a structured framework to maintain timelines and budgets.
Open communication
We value open, transparent communication with clients and within our team—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, 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 patient insights 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 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®.
Discover moreMeet our team of solution-oriented project managers
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 undoubtley 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.
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