Vivatiq Clinical Research is committed to maintaining high standards of quality, ethics, and regulatory compliance across all clinical trial activities. We adhere to internationally recognized clinical research guidelines to ensure patient safety, ethical conduct, and the generation of accurate, reliable, and audit-ready data. Our standardized processes, robust documentation practices, and dedicated quality oversight help ensure consistent compliance, data integrity, and smooth regulatory inspections throughout the study lifecycle.
Accelerating Clinical Research with Precision and Integrity
The focus is on driving medical innovation through precise, ethical, and patient centric clinical trials.With expertise across multiple therapeutic areas and a strong presence at multiple sites across India, Vivatiq supports sponsors from early development to post marketing studies.
Why to Choose Vivatiq ?
VIVATIQ Clinical Research is a Bangalore-based clinical research service provider partnering with pharmaceutical, biotech, nutraceutical, and medical device companies to deliver end-to-end clinical trial solutions across Phases I–IV. In 2025, Our Site successfully underwent a DCGI inspection, reinforcing its commitment to regulatory compliance, quality standards, and ethical clinical research practices.
Experience and Expertise
Our team brings 25+ years of combined experience in clinical research and successfully cleared a DCGI audit in 2025, reflecting our strong compliance and quality standards.
Quality focused
Strong quality systems ensure regulatory compliance while safeguarding data integrity and patient safety throughout the trial lifecycle.
Technology Enabled
Advanced clinical trial software and data management tools streamline trial operations, improve data accuracy, and enhance transparency across all study activities.
Patient Centric
Processes and protocols are carefully designed to protect patient rights, ensure safety, and support long-term well-being throughout every stage of the clinical study.
Services
End to End Clinical Research Services
Vivatiq offers a full spectrum of clinical trial services from planning and protocol development to execution, monitoring, data analysis, and regulatory reporting across phases I–IV.
Therapeutic Expertise & Process
Vivatiq has experience supporting clinical trials across a broad range of therapeutic specialties, enabling us to address diverse study requirements with scientific rigor and operational excellence. Our team combines therapeutic knowledge with regulatory and ethical compliance to deliver reliable outcomes at every stage of clinical development.
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Endocrinology
Vivatiq supports endocrinology studies in diabetes, thyroid, and hormonal disorders, with a focus on accurate metabolic assessment and patient safety.
Cardiology
Expertise in managing clinical trials for hypertension coronary artery disease heart failure arrhythmias and lipid disorders with strict adherence to regulatory and ethical standards.
Infectious Diseases
We supports infectious disease clinical trials across bacterial, viral, and parasitic conditions, with a strong focus on accurate diagnostics, patient safety, and regulatory compliance.