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SFDA Hold GMP Implementation Work Symposium
Release time: 2011-02-23 & nbsp & nbsp & nbsp Source:

February 18,The State Food and Drug Administration organizes the pharmaceutical industry association and pharmaceutical manufacturer,Hold GMP Implementation Work Symposium,Notified the relevant situation and implementation plan of the new version of GMP,Broadly listening stake online sports bettingto the opinions and suggestions of the next implementation work in the industry。

 

Sun Xianze, Director of the Director of the Drug Administration of the State Food and Drug Administration, introduced the revision characteristics of the new version of GMP and the comprehensive consideration and preliminary arrangement of the National Bureau for implementation。

 

Sun Xianze said,The National Bureau attaches great importance to the implementation of the new version of GMP,After the implementation of the new version of GMP, it may investigate and evaluate the impacts of the industry and enterprises.。Considering that the company conducts relevant training on new standards、Establish a quality management system、Prepare technical reform and time required for construction,It is determined that the transition period for 3 years to give existing pharmaceutical manufacturers will be given to the original soliciting opinion draft,Extension to a transition period that does not exceed 5 years,and according to the degree of product risk,Requires the requirements of the new version of GMP according to the category。For newly -built drug manufacturers、Drug production stake betting appenterprises newly built (change、Expansion) The workshop is required to meet the requirements of the new version of GMP from March 1, 2011。Sun Xianze hopes that the company will actively act,Preparations for early,Relevant training work is carried out as soon as possible in accordance with the standard requirements,Improve management level,Strengthen the GMP consciousness of all personnel,Establish the whole process、All -in -one、Dynamic quality management concept,Strive to pass the certification of the new version of GMP as soon as possible。

 

Participating in the meeting is the China Chemical Pharmaceutical Industry Association、China Medical Quality Management Association、China Chinese Medicine Association、China Medical Equipment Engineering Association related industry associations and Shenwei Pharmaceutical、Harbin Pharmaceutical Group、North China Pharmaceutical、Representatives of drug manufacturers such as Xinhua Pharmaceutical。All companies attending the meeting said that they should actively study and implement the new version of GMP,And believes that the 5 -year transition Stake Sports Bettingperiod given by the National Bureau in the implementation fully considers the actual situation of the enterprise,All have confidence to meet the requirements of the new version of GMP within the required period。

 

Will on the way,Corporate representatives also hope that the country is in drug prices、Bidding and other aspects can introduce related supporting and support policies,Actively implement、Enterprises that strive for the new version of GMP certification will be encouraged。

 

National Development and Reform Commission、Department of Industry and Information Technology、The relevant responsible comrades of the Ministry of Health and other ministries and commissions attended the symposium on the same day,I listened to the Industry Association、Production enterprises' opinions and suggestions on the implementation of the new version of GMP。