Quality Assurance

Naturotac is committed to deliver quality and regulatory compliant clinical trial services in a professional, efficient, timely and cost-effective manner while protecting patient safety and data integrity for regulatory submissions.

Naturotac offers the Quality Assurance (QA) services in GCP domains in line with applicable GxP regulations. Quality assurance auditors have expertise in local, national and international regulations, standards and guidelines.

Key Strengths:

Independent quality assurance function reporting to management for all in-house Clinical and Bioanalytical studies.
Well structured QA audits at pre-defined intervals to ensure data integrity
Regular system audits to facilitate continuous system improvements
Handle regulatory/sponsors queries, recommendations through corrective/preventive actions, modifying and implementing our systems and processes wherever required
Conduct internal audits of study activities and data/reports and ensuring compliance as indicated by acceptance of the product dossiers (Regulatory submissions) by regulatory agencies
Manage sponsor audits for assessment of Naturotac facilities & GCP/GLP compliance
Dedicated, qualified & well trained QA auditors
Teams with well defined job responsibilities for conducting internal audits, document control and archival activities
Fire proof and access controlled Archival facility which is situated within QA department.

Quality Assurance

Key Strengths:

About Us

Services

Contact Us