Based on the China Drug Administration Regulations, the Good Manufacturing Practice (GMP) and Good Supply Practice (GSP) list the mandatory requirements and basic guidelines covering pharmaceutical products manufacturing and quality control to ensure the safety and quality of these products and reduce the risks in their distribution. In this aspect, GMP certification can help improve the overall level of pharmaceutical production management, while GSP can enhance the pharmaceutical trading  situation and its supply chain system.

The new versions of GMP2010 / GSP2013 have been released and implemented for some time and enterprises engaged in this sector must be aware of these new requirements. Enterprises that do not meet the requirements of the new guidelines would risk not being able to continue their production. Upgrading their production standard is necessary to receive these certifications.

Testo product application engineer, Mr. Guo Weimin, will talk in detail about the GMP and GSP regulations, and how to meet the new guidelines. He will also talk about other important aspects of production such as the use of portable measuring instruments, testo wireless temperature and humidity monitoring systems for data monitoring, data archiving, alarm management, data traceability, electronic signatures, etc.

On September 22, 2015 from 14:00 - 15:00, we look forward to your participation!  For more information or to register, click here.(The webinar is in Chinese.)


Key topics:
1. Introduction on GMP and GSP regulations
2. Measuring equipment part solutions
3. Authentication service part solutions
4. Calibration device part solutions