Fueled by a deep-rooted passion for precision and regulatory excellence, we empower pharmaceutical, biotechnology, medical device, semiconductor industries and scale-up support for pharmaceutical manufacturing facilities for organizations ranging from ambitious startups to global enterprises to thrive in highly regulated environments. Our comprehensive service portfolio includes end-to-end project lifecycle management, turnkey cleanroom design and construction, equipment qualification, validation services, laboratory infrastructure development, QMS architecture and implementation, vendor qualification, and full-spectrum regulatory alignment. We also provide end-to-end support for obtaining critical regulatory approvals such as US FDA 510(k), CE Certification, CDSCO registration, CDSCO import and manufacturing licenses, and other global certifications streamlining your path to market and compliance.

Explore our website to discover how Micron can accelerate your journey toward regulatory success and operational transformation.