Pacific Meinuoke Biopharmaceutical

Facilities

Pacific Meinuoke follows all Current Good Manufacturing Practices (cGMP) which are prescribed for pharmaceutical manufacturers to ensure their products produced are in accordance of the specific requirements for identity, strength, quality and purity while every practice of Pacific Meinuoke is also strictly complying with all the requirements of Chinese State Food and Drug Administration (SFDA) to guarantee that our customers always receive the highest quality biologics.

The company now has set up 2 production lines ( 5 to 30 liters and 5 to 300 liters ), and is presently building two EMEA (European Medicines Agency) compliant production lines for fermenting, purifying and manufacturing from 5 to 3,000 liters.