• Located in Tai Po Industrial Estate, N.T., Hong Kong
  • Gross Area greater than 77,000 sq. ft.
  • Clean Room Area for manufacturing more than 32,000 sq. ft.
  • Clean Room Area fulfilled Class 10,000 and Class 100,000 standard
  • Fulfilled the WHO standards for Good Manufacturing Practices for pharmaceutical products
  • Completed and in full operation since April, 2003
  • Equipped with a tablet manufacturing line, a capsule manufacturing line, an oral syrup/liquid manufacturing line, an external liquid
  • manufacturing line, a cream/ointment manufacturing line, an eye drops manufacturing line, and an antibiotic manufacturing line
  • In-house Quality Control Laboratory