Basing on the economic analysis of railway's natural monopoly, we begin from the foreign models to analyze the experiences of America and England. We give some advice on price regulation of China railway industry fro...Basing on the economic analysis of railway's natural monopoly, we begin from the foreign models to analyze the experiences of America and England. We give some advice on price regulation of China railway industry from fixing price method, supervised objects, patterns and institution.展开更多
Within the public health sector of Hong Kong(China),there is a consensus around the important role of traditional Chinese medicines.For Hong Kong(China)to play a bridging role to bring Chinese medicines to the global ...Within the public health sector of Hong Kong(China),there is a consensus around the important role of traditional Chinese medicines.For Hong Kong(China)to play a bridging role to bring Chinese medicines to the global market requires a concerted effort from the government,academic institutes and industries.The release of the final version of the European Medicines Agencies guidance document,which details the acceptance of minimum requirements to nonclinical package in bibliographical applications,grants the opportunity for well-established and traditional herbal medicines to demonstrate an‘acceptable safe’status for registration in the European Union.It is anticipated that this minimum nonclinical package can be applied to demonstrate the safe use of many traditional Chinese medicines regardless of their eligibility to be registered under the simplified procedure within the European Union.This paper conceptualizes an integration of a simplified evaluation route for eligible proprietary Chinese medicines(pCm)with long history of use into the existing drug regulatory framework in Hong Kong(China).Such integration utilizing the minimum nonclinical package,based on bibliographical data or expert report,as proof of evidence to demonstrate safety for pCm with long history of use requires less demand in scientific resources.With Hong Kong(China)conducting‘first hand’review for eligible pCm,it provides an option for overseas and local pharmaceutical companies to register their products in Hong Kong(China)without the need to rely on issuance of Certificate of Pharmaceutical Product from other countries.This could bring eligible pCm with long history of use to reach international risk-based standard and to be marketed globally as‘medicines’to reach their full therapeutic potential.An important process to positioning Hong Kong(China)to compete with other countries in promoting importation and exportation of pCm to better serve the global health.展开更多
The processing trade has, since 1996, taken half of the total import and export trade value for a consecutive six years. Despite the impact and influence of the Asian financial crisis, it has maintained a momentum of ...The processing trade has, since 1996, taken half of the total import and export trade value for a consecutive six years. Despite the impact and influence of the Asian financial crisis, it has maintained a momentum of steady growth. In the five years from 1997 to 2001, import and export value through the processing trade grew at an annual average rate of 10.5 percent, with exports growing at an annual average rate of 11.8 percent. This good growth momentum continued into展开更多
文摘Basing on the economic analysis of railway's natural monopoly, we begin from the foreign models to analyze the experiences of America and England. We give some advice on price regulation of China railway industry from fixing price method, supervised objects, patterns and institution.
文摘Within the public health sector of Hong Kong(China),there is a consensus around the important role of traditional Chinese medicines.For Hong Kong(China)to play a bridging role to bring Chinese medicines to the global market requires a concerted effort from the government,academic institutes and industries.The release of the final version of the European Medicines Agencies guidance document,which details the acceptance of minimum requirements to nonclinical package in bibliographical applications,grants the opportunity for well-established and traditional herbal medicines to demonstrate an‘acceptable safe’status for registration in the European Union.It is anticipated that this minimum nonclinical package can be applied to demonstrate the safe use of many traditional Chinese medicines regardless of their eligibility to be registered under the simplified procedure within the European Union.This paper conceptualizes an integration of a simplified evaluation route for eligible proprietary Chinese medicines(pCm)with long history of use into the existing drug regulatory framework in Hong Kong(China).Such integration utilizing the minimum nonclinical package,based on bibliographical data or expert report,as proof of evidence to demonstrate safety for pCm with long history of use requires less demand in scientific resources.With Hong Kong(China)conducting‘first hand’review for eligible pCm,it provides an option for overseas and local pharmaceutical companies to register their products in Hong Kong(China)without the need to rely on issuance of Certificate of Pharmaceutical Product from other countries.This could bring eligible pCm with long history of use to reach international risk-based standard and to be marketed globally as‘medicines’to reach their full therapeutic potential.An important process to positioning Hong Kong(China)to compete with other countries in promoting importation and exportation of pCm to better serve the global health.
文摘The processing trade has, since 1996, taken half of the total import and export trade value for a consecutive six years. Despite the impact and influence of the Asian financial crisis, it has maintained a momentum of steady growth. In the five years from 1997 to 2001, import and export value through the processing trade grew at an annual average rate of 10.5 percent, with exports growing at an annual average rate of 11.8 percent. This good growth momentum continued into