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- 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
  
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