Mfg. License B Application
Mfg. License B Application

Pharmaceutical Manufacturing Certificate (B) is the qualification certificate for obtaining a drug production license when MAH adopts the form of commissioned production (such as when a R&D institution entrusts a pharmaceutical manufacturer to carry out production), and it is also one of the necessary materials for drug registration application.

Beijing Canny Consulting Inc. has successfully guided 9 R&D enterprises to obtain the " Pharmaceutical Manufacturing Certificate " (B), all of them one-time passed the inspection, and two of them "zero defect" through the official inspection. 

For more than 20 years, the company has formed a mature and standardized service system in terms of consultant team, service standards, service procedures, project management, confidentiality system, etc., and has passed ISO 9001 quality management system certification for many consecutive years, becoming the earliest consulting company in the field of drug administration and regulations that passed ISO in China.

CANNY-Your Trustworthy Consultant for Drug Regulatory Compliance!
  • 25 years
    of professional consulting experience in the pharmaceutical industry
  • 700 +
    GMP certification projects for China, EU, FDA, UK, Japan, Australia and WHO inspection
  • 320 +
    Validation execution and guidance projects
  • 2400 +
    Globally RA registration projects
  • 1370 +
    Globally clients and pharmaceutical partners
  • 30 +
    Experts from China, US and EU
Professional Services, Standardized SOPs

Providing full-life cycle solutions for MAH project

If you have business needs
Contact Us