Regulatory Services Worldwide

We are committed to assisting manufacturers both home and abroad to gain reliable and rapid access to the registration certificate in Europe, the US and other countries for their products with our professional, standardized and timely technical consulting services of high quality. Our professional team, characterized as good command of foreign languages and familiarity with domestic and international laws and regulations on pharmaceuticals, has abundant experience in pharmaceutical production, quality management and years of practice in technical consulting services for pharmaceutical products. Over the years, we’ve been cooperating with European/ US experts, which ensures the authoritativeness of our services.

Our services

• Regulatory Documentation
  • EDMF
  • DMF
  • COS/CEP
  • Other documentation – SMF/PMF
• FDA/EU-GMP inspection
• Vendor audit of GMP compliance
• In-House Training Services
• Laboratory Technology Services

Contact