Qinfu Technology has a beautiful landscape of its own-they are respectable and lovely devotees and unknown strugglers. Summer is hot, and under the high temperature of 40 degrees, everyone sticks to their posts, with hardships, sweat and joy of harvest.

Thanks for this factory group building, through the group building activities, we have established a closer relationship and made the team a big family. I believe that with the joint efforts of everyone, Lufu Technology will get better and better!

Create a temperature and humidity environment needed for drug failure evaluation by scientific methods, which is suitable for the experiment of influencing factors of drugs and new drugs in pharmaceutical enterprises.

Create a temperature and humidity environment needed for drug failure evaluation by scientific methods, which is suitable for the experiment of influencing factors of drugs and new drugs in pharmaceutical enterprises.

On July 11-12, we met in Wuhan Optics Valley Biological Innovation Park Convention Center, booth No.2.

To create a scientific method for the drug failure evaluation of the required temperature, humidity, light environment, applicable to pharmaceutical enterprises on the drug and new drug influence factors experiment. Configure a three-level authority and audit trail electronic records system. Complies with North American FDA 21CFR PART 11 regulations and is suitable for CGMP certified users.

The QF-SD-3T series provides a stable and reliable temperature and humidity environment, is specially designed for the pharmaceutical industry for drug stability testing to check that the drug has met the expiration date, is equipped with a three-level authority and audit trail electronic record system, complies with North American FDA 21CFR PART 11 regulations, and is suitable for CGMP certified users.

The QF-SD-3T series provides a stable and reliable temperature and humidity environment, is specially designed for the pharmaceutical industry for drug stability testing to check that the drug has met the expiration date, is equipped with a three-level authority and audit trail electronic record system, complies with North American FDA 21CFR PART 11 regulations, and is suitable for CGMP certified users

To create a long-term temperature and humidity environment for drug failure evaluation in a scientific way. Convenient storage of large quantities of drugs, as well as long-term moisture cycle testing.