Who We Are
CLINIGMA® makes patient-centered research easy for pharmaceutical companies—putting authentic patient voices at the core of drug development. Our dedicated team of global professionals deliver ICH-GCP compliant patient research for robust regulatory evidence.
Market-leading patient experience research
We are a dynamic team of dedicated professionals who make patient feedback easy. We've built a forward-thinking company to transform how the pharmaceutical industry listens and learns from the people who matter most—patients. We've grown from passionate advocates to market leaders in patient-centered drug development.
From vision to leadership
What began as a commitment to authentic patient voices has evolved into industry-leading expertise. Through our continued commitment to rigorous global qualitative research and cutting-edge technology, we amplify patient voices across cultures, languages, and continents.
From the outset, we have prioritized ICH-GCP compliant interview solutions, valuing in-depth insights, patient safety, ethical conduct, data security, and integrity. By delivering high-quality services, we have become a preferred provider of patient experience research and consultancy for many leading pharmaceutical companies.
Every project teaches us something new. Every challenge drives us to innovate. This continuous evolution is how we've become market leaders—by constantly raising the bar for ourselves and our industry.
Making complex research easy
We make in-trial interviews simple while ensuring ICH-GCP compliance—facilitating the entire process from protocol development to reporting and regulatory submissions. Our solution-oriented approach combines:
Market-leading interview portal
The CLINIGMA® Portal streamlines the research process for easy and secure data collection, in compliance with ICH-GCP, ALCOA++ principles and data privacy laws.
Scientific expertise
Our experienced team of industry experts understand how to navigate the complex landscape of patient evidence for regulatory submissions.
Regulatory compliance
All patient research is conducted in compliance with ICH-GCP to uphold the highest ethical and regulatory standards.
Cultural intelligence
Deep understanding of global markets and cultural nuances that affect patient experiences and data fidelity.
Personalized service
Tailored solutions in alignment with your project objectives, timelines, and unique requirements.
Operational excellence
CLINIGMA® is ISO9001:2015 certified in designing, conducting, analyzing and reporting patient interviews in relation to clinical trials.
Quality without compromise
Your research deserves quality without compromise. Our meticulous attention to detail and forward-thinking outlook, ensure we keep you ahead of regulatory and industry trends. As your strategic partner, we deliver a high quality service that translates into successful submissions and authentic patient-focused drug development.
The team behind your success
Our growing international in-house team and extended network of 300+ professionals bring a wealth of expertise. From seasoned industry experts to anthropologists, regulatory specialists and technology innovators, our diverse team shares one trait: enthusiasm for the work we do. This passion is evident in every project we deliver. Our dedication shines through the quality of insights we generate and the relationships we build with our clients.
Patient research made easy
Work with our dedicated team of professionals to make patient experience research simple and rewarding.
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