According to the recently held at the 2012 National Food and Drug Supervision stake online sports bettingand stake online sports bettingAdministration Conference, it was learned，154 pharmaceutical manufacturers across the country have passed the newly revised drug GMP certification inspection。The State Food and Drug Administration (hereinafter referred to as the National Bureau) Shao Mingli emphasized at the meeting，Be careful of the implementation of the newly revised drug GMP，Perseverance does not relax when the time limit、Standard does not decrease。

According to an introduction，Among the 154 companies that have passed the certification，88 are certified by the State Administration，The certified dosage form is mainly injection、Biological Products。66 enterprises that have been certified by the provincial bureau，The authentication dosage form is mainly concentrated in Chinese medicine drinks、APIP、tablets、Capsules, etc.。Current，The main certification is large、Middle -size Enterprise。

The newly revised drug Stake Sports BettingGMP stake betting appis to protect advanced productivity、Eliminate backward productivity、Promoting industrial structure adjustment、Major measures to enhance the international competitiveness of my country's pharmaceutical industry。The newly revised pharmaceutical GMP is also faced during the implementation process: some companies are waiting to wait and see、Reconstruction process is greedy for all、Insufficient input of software and personnel，Individual regulatory agency capabilities are insufficient。To stake betting appPromote the implementation work，Guarantee implementation on time，Promoting the implementation of the new revised drug GMP has been listed as one of the main points of food and drug supervision and management in 2012。The State Administration will recently issued the "Opinions on Strengthening the Implementation of Drug Production Quality Management (Revised in 2010)，Category Guidance Stake Sports BettingEnterprise Promote the implementation of newly revised drugs GMP。The National Bureau will also strengthen the guidance and management of provincial certification work，Carry out supervision and spot checks on the certification work of the provincial bureau。

Shao Mingli requested that in 2012, we must seriously do the GMP implementation of the newly revised drugs。Food and drug supervision departments at all levels should follow the overall arrangement of the drug GMP step by step，Perseverance does not relax when the time limit、Standard does not decrease，Strengthening the supervision and guidance of manufacturers，Strict on -site inspection，Guarantee standard uniform，Make sure the certification quality and efficiency。