Port communicationNationwide operations and the inability to apply for new ones make pharmaceutical wholesale licenses highly valuable.，The market transfer price is over several million。Some of the transferred companies have warehouses、address、Assets packaged together，There are also single company and license transfers，Depend on buyer’s needs。
Drug business licenses are divided into retail and wholesale categories.，The retail category refers to the licenses that offline chain pharmacies such as Changsheng Pharmacy need to apply for.，In the wholesale category, drug companies need this license to wholesale drugs to pharmacies or other medical institutions with retail licenses.。
According to the provisions of the "Opinions of the Supreme People's Court on Several Issues Concerning the Trial of Administrative Cases concerning Authorization and Confirmation of Trademark Rights"，The People's Court examines and determines whether the disputed trademark is a generic name，Generally, the factual status at the time of filing the trademark registration application shall prevail.。
If it is not a common name at the time of application，However, the disputed trademark has become a common name when the registration is approved.，It should still be recognized as belonging to the common name of the product;Although it was the common name of this product at the time of application，However, it is no longer a common name when the registration is approved.，does not prevent it from obtaining registration。therefore，Determine whether the drug belongs to the generic name，The actual status at the time of registration approval shall prevail.。
At present, my country's national drug standards include the Pharmacopoeia of the People's Republic of China、Drug standards promulgated by the State Food and Drug Administration、Drug registration standards and drug trial standards promulgated by the State Food and Drug Administration，The drug names included in the above standards are all common drug names.。
Regarding drug trial standards issues，2007In the newly promulgated "Measures for the Administration of Drug Registration" on June 18,，The content of the original "Measures for the Administration of Drug Registration" regarding drug trial standards has been cancelled.。
subsequently，According to the "Notice on Matters Concerning the Implementation of Drug Registration Management Measures" promulgated by the State Food and Drug Administration on September 26, 2007,，2007From October 1，Varieties approved for production according to the new "Measures for the Administration of Drug Registration"，Its drug standards are official standards。
Previously approved drug trial standards，Still in accordance with the original "Measures for the Administration of Drug Registration" regarding the procedures and procedures for converting drug trial standards into regular versions
Require
，Apply for and handle the formalization of drug trial standards。therefore，From October 1, 2007，There will no longer be new “drug trial standards” in our country。
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