Only 10% inland pharmaceutical enterprises passed the certification for new edition GMP in 2013, 70% enterprises need transforming and upgrading, and the expenses for upgrading from 6 million to 10 million, among them, there are lots of input in the remolding for equipment.
The new edition drugs GMP improve the requirements of sterility and purification in the productive process. This is not only put forward requirements for the facilities of drug manufacturing enterprises, but also come up with relevant requirements for the design, manufacture, and installment of the productive equipment which used in sterile link. 2014 will become the reform starting year for new edition GMP in pharmacy.
In order to learn the GMP Regulations amended in 2010 and drugs companies accreditation transformation of completion, communicate the newest pharmacy technologies and equipment skills at home and abroad, discuss how to deal with the requirements of transformation and upgrade according to new edition GMP for the pharmacy enterprises,”2014 China Pharmaceutical Industry Summit” will be hold in Shanghai from 3th to 4th July 2014.