Purpose of implementing prevent mix between different drugs or their components; to prevent cross-contamination by other drugs or other substances brought; prevent errors and distortion measurement transfer and information transfer; omission of any biological and verification steps to prevent accidents; prevent any operation and not the implementation of standards and lower limit feeding and other illegal illegal accident; the main purpose of the development and implementation of 高标准 is to protect the interests of consumers what Nansha 高标准, to ensure safe and effective medication people; but also to protect the drug manufacturers, so that enterprises have Laws to Follow, rule; in addition, the implementation of 高标准 and the law gives the government responsibility in the pharmaceutical industry, and also after China's accession to WTO, implementation requires pharmaceutical quality assurance system - because if not by pharmaceutical manufacturers 高标准 certification Nansha What is 高标准, may be refused on the outside of technical barriers to international trade. New 高标准 and regulatory approval, drug recalls, adverse reaction monitoring and other aspects of regulatory requirements is how effective convergence? New 高标准 stressed and drug registration, drug recalls, adverse drug reaction monitoring other regulatory aspects of effective convergence. Production quality management process for regulatory approval of drugs is required to implement and reflect. In several chapters of the new 高标准 "production management", "quality management", "commissioned the production and inspection commission" and has emphasized the conformity of production requirements and regulatory approval requirements. New 高标准 also note with "drug recall management approach" convergence, enterprises should formulate provisions recall procedures, designate a person responsible for organizing and coordinating the work of the Nansha recall what is 高标准, urge enterprises in accordance with the provisions of "drug recall management approach", after the listing of drugs Once the quality problems or injury event occurs, can the first time to recall all the problems of drugs, to avoid new hazards. Adverse drug reaction monitoring Nansha What is 高标准, in the 1998 edition 高标准 relevant provisions in there, but the provision is very simple. In the new 高标准 enterprises should establish clearly defined adverse drug reaction reporting and monitoring and management system, the initiative to collect adverse reaction, and the establishment of specialized agencies, with full-time staff in charge of management. These provisions are being revised and will soon promulgate and implement the requirements of "adverse drug reaction reporting and monitoring management approach" is consistent. Guangdong 高标准 certification, enterprises of the Road (online consultation), Nansha 高标准 provided by enterprises in Huizhou City Road Enterprise Management Services Limited. Guangdong 高标准 certification, enterprises of the Road (online consultation), Nansha 高标准 is half way Huizhou City Enterprise Management Services Ltd. (isoew.com) this year introduced a new upgrade, the above picture is for reference only, please call or pictures on this page contact telephone number, to obtain the latest information, Contact: Miss Shi.