ISO 13485 Certified · CE Marked · CDSCO Approved

Trusted Medical Engineering Partner

20+ years of innovation in medical device manufacturing, serving 50+ countries with state-of-the-art facilities and unwavering quality standards.

  • Quality & price advantage over competitive brands
  • A front-runner in the global medical device industry
20+
Years of Excellence
50+
Countries Served
500+
Clients Worldwide
10M+
Units / Year

Why George Philips?

Four pillars that make us the preferred manufacturing partner for medical device companies worldwide.

Quality & Compliance

ISO 13485 certified Quality Management System. CE marked products complying with EU MDR. Rigorous in-process and final product testing.

Manufacturing Scale

50,000 sq ft state-of-the-art facility with ISO Class 7 & 8 cleanrooms and capacity exceeding 10 million units per year.

Global Reach

Trusted by 500+ clients across 50+ countries. Strong distributor network and regulatory documentation support for market entry.

Cost Effectiveness

Competitive pricing without compromising quality. Leverage India manufacturing advantages while maintaining global compliance.

20+
Years of Excellence
50+
Countries Served
500+
Clients Worldwide
10M+
Units/Year Capacity

Regulatory Certifications & Compliance

ISO 13485:2016Quality Management System
CE MarkEuropean Conformity
CDSCOCentral Drugs Standard Control
WHO-GMPGood Manufacturing Practice
FDA Ready510(k) Documentation

Ready to Partner with Us?

Whether you need OEM manufacturing, product sourcing, or a long-term supply agreement — our team is ready to help.