Get in Touch
Reach out to CliniGenix for inquiries regarding clinical trial services, collaborations, or regulatory support. Our team will respond within 24–48 hours.
Contact Information
Get in touch with us through any of the following channels
Office Address
CliniGenix Ltd.
C-46, Sector-62,
Noida – 201301,
Uttar Pradesh, India
Phone
Primary
+91 8595806530Working Hours
Mon–Fri, 9 AM – 6 PM IST
Support
support@clinigenix.comResponse time: 24–48 hours
Locate Us
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CliniGenix Ltd. • C-46, Sector-62, Noida – 201301, Uttar Pradesh, India
Frequently Asked Questions
Find answers to common questions about our services and partnerships
Clinigenix supports a wide range of clinical trials across all phases (Phase I-IV), including oncology, cardiology, neurology, rare diseases, and more. We provide end-to-end services from protocol development to regulatory submissions and post-market surveillance.
Our team typically responds to all business inquiries within 24–48 hours. For urgent matters or time-sensitive proposals, we can arrange expedited consultations to ensure your project timelines are met.
Absolutely! We actively collaborate with principal investigators, research institutions, and hospitals. Our partnerships are designed to support your research goals while ensuring compliance with regulatory standards and ethical guidelines.
Yes, we provide comprehensive regulatory support including IND/NDA submissions, clinical trial applications (CTAs), ethics committee submissions, and ongoing regulatory maintenance. Our team has extensive experience with FDA, EMA, and other global regulatory bodies.
Clinigenix operates globally with expertise in North America, Europe, Asia-Pacific, and emerging markets. We have experience navigating diverse regulatory landscapes and can support multi-regional clinical trials.