Quality Assurance
Quality & Compliance
Vivatiq Clinical Research is firmly committed to maintaining the highest standards of quality, ethics, and regulatory compliance across all clinical trial activities. The organization strictly adheres to internationally recognized clinical research guidelines, including ICH-GCP, applicable regulatory authority requirements, and ethical principles that safeguard patient rights, safety, and well-being throughout the study lifecycle.
All trial processes are designed to ensure the generation of scientifically rigorous, accurate, and reliable data that are fully traceable and audit-ready. Vivatiq implements standardized operating procedures (SOPs), robust documentation practices, and controlled data management systems to support data integrity and transparency at every stage of clinical development.
A dedicated Quality Assurance (QA) team independently oversees trial operations through regular internal audits, process reviews, and compliance checks. This proactive approach helps identify potential risks early, implement corrective and preventive actions (CAPA), and continuously improve operational performance. Through rigorous quality oversight and a culture of compliance, Vivatiq ensures that every study meets regulatory expectations and supports successful regulatory submissions.