SFDA issued regulations to strengthen the quality supervision of basic drugs
Release time: 2009-10-22 & nbsp & nbsp & nbsp Source:
A few days ago，SFDA issued stake sports betting appMy stake betting app"Regulations on Strengthening the Supervision and Management of Basic Drug Quality" (hereinafter referred to as the "Regulations")，Put forward the evaluation of drug standards for basic drugs; strengthen the production verification of basic drugs; implement full varieties of basic drugs;。
According to the "Regulations"，Basic drug manufacturers should take the initiative to carry out the research and revision of drug standards。The National Bureau will evaluate the drug standards of basic drugs one by one，Accelerate the improvement of basic drug standards。For the need for the standard，Basic drug manufacturers shall complete the standard revision work in accordance with the requirements; there are different standards for the same drug，Uniformly increase the principle of standard advancedness。Standards for basic drugs My stake betting appstake sports betting appare given priority to Chinese Pharmacopoeia。
Regulations requirements，Basic drug manufacturers should be produced in strict accordance with the drug GMP，Establish and implement the quality of the quality authority，Improve quality management、Strengthening the construction of risk control system。The state encourages and promotes the merger and reorganization of basic drug distribution companies、Integrated distribution resources，Develop modern logistics，Improving drug distribution ability。Medical institutions and retail pharmacies must strengthen the purchase of basic drugs、Acceptance、Storage、Deployment and other links management。The National Bureau will increase the ratio of basic drugs in the annual drug drawing plan，Provincial drug regulatory authorities do at least one test of basic drugs stake online sports bettingstake sports betting appproduced by basic drug manufacturers in the area each year。
"Regulations" is also clear，Relevant units involving basic drugs shall establish and improve the adverse reaction report and processing system，Drugs that have hidden safety hazards shall be recalled in time in accordance with regulations。State Administration organizes to carry out basic drug varieties and basic drug variet，and gradually incorporate basic drugs into drug electronic supervision。
