Globesynth Pharma Tech is firmly committed to consistently meeting and exceeding customer expectations by delivering high-quality products and services in a timely and compliant manner. Our quality philosophy is built on scientific rigor, operational excellence, and continual improvement through ongoing enhancement of technical competencies, process controls, and domain knowledge.
A robust Quality Management System (QMS) is established and effectively implemented across all operations through structured training programs, documented procedures, and a culture of teamwork and accountability. Continuous process improvement and risk-based thinking form the foundation of our quality-driven approach.
Our facilities are ISO 9001:2015 certified, accredited by URS Certifications and NABCB, ensuring systematic control over quality, consistency, and customer satisfaction. As part of our commitment to analytical excellence, our quality systems are being progressively enhanced in alignment with ISO/IEC 17025:2017 requirements for testing and calibration laboratories.
All analytical and research activities at Globesynth Pharma Tech strictly adhere to current Good Laboratory Practices (cGLP). Our analytical laboratories are duly approved by the Food and Drug Authority (FDA), Government of Tamil Nadu, and the Central Drugs Standard Control Organisation (CDSCO), reinforcing our compliance with national regulatory standards.
Through scientific integrity, regulatory compliance, and continuous innovation, Globesynth Pharma Tech remains dedicated to maintaining the highest standards of quality across research, development, and manufacturing services.
Globesynth Pharma Tech — Quality first, always.