1.0https://vivatiqclinicalresearch.comvullikantivinay2627@gmail.comhttps://vivatiqclinicalresearch.com/?author=1rich600338<blockquote class="wp-embedded-content" data-secret="zswO32zxIq"><a href="https://vivatiqclinicalresearch.com/">Home</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="https://vivatiqclinicalresearch.com/?embed=true#?secret=zswO32zxIq" width="600" height="338" title="“Home” — " data-secret="zswO32zxIq" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script> /*! This file is auto-generated */ !function(d,l){"use strict";l.querySelector&&d.addEventListener&&"undefined"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!/[^a-zA-Z0-9]/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret="'+t.secret+'"]'),o=l.querySelectorAll('blockquote[data-secret="'+t.secret+'"]'),c=new RegExp("^https?:$","i"),i=0;i<o.length;i++)o[i].style.display="none";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute("style"),"height"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):"link"===t.message&&(r=new URL(s.getAttribute("src")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener("message",d.wp.receiveEmbedMessage,!1),l.addEventListener("DOMContentLoaded",function(){for(var e,t,s=l.querySelectorAll("iframe.wp-embedded-content"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute("data-secret"))||(t=Math.random().toString(36).substring(2,12),e.src+="#?secret="+t,e.setAttribute("data-secret",t)),e.contentWindow.postMessage({message:"ready",secret:t},"*")},!1)))}(window,document); //# sourceURL=https://vivatiqclinicalresearch.com/wp-includes/js/wp-embed.min.js </script> 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 completed the 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 inspectionin 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. ABOUT US Advancing Clinical Research with Integrity and Excellence Vivatiq Clinical Research is a Bangalore-based site management organization dedicated to delivering high-quality and ethical clinical research services. Founded in 2021 and led by a team with over 25 years of combined experience, we support pharmaceutical, biotechnology, nutraceutical, and medical device companies across all stages of clinical development. Read More 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.​ Clinical Trial Managment Clinical trial management involves planning, coordinating, and overseeing clinical studies to ensure they are conducted efficiently, ethically, and in compliance with regulatory and GCP standards. Medical Writing Medical writing involves creating clear, accurate, and compliant clinical and regulatory documents, including study reports, protocols, and submissions. Project Management Vivatiq ensures trial success through precise budgeting, rigorous milestone tracking, and transparent sponsor communication to maintain total alignment and timeline adherence. View All Services 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. No Data Found No Data Found 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. Read More Our Process & Clients A Comprehensive, Step-by-Step Process for Reliable and Compliant Clinical Research At Vivatiq Clinical Research, our structured  process supports the successful execution of clinical trials with a strong focus on quality and compliance. We collaborate closely with sponsors to develop scientifically sound protocols, identify and initiate high-performing sites, and implement effective patient recruitment and retention strategies. Through continuous monitoring and operational oversight, we ensure patient safety, data integrity, and adherence to regulatory guidelines. Our comprehensive data analysis and reporting capabilities deliver reliable, regulatory-ready results that support confident clinical and business decisions. VIEW MORE Quality Assurance Quality & Compliance 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.      Read Morehttps://vivatiqclinicalresearch.com/wp-content/uploads/2025/12/about-us-image.png10801080