2.GSP is the abbreviation of "Quality Management Standard for Pharmaceutical Trading", which is a unified quality management standard for pharmaceutical trading enterprises. A pharmaceutical trading enterprise shall meet the GSP requirements within the time specified by the pharmaceutical supervisory and administrative department, and obtain the certification certificate through certification.
Difference:
1, different requirements
GMP requires pharmaceutical, food and other production enterprises to have good production equipment, reasonable production technology, perfect quality management and strict testing system to ensure that the final product quality (including food safety and hygiene) meets the requirements of laws and regulations.
GSP is a set of management procedures to control all factors that may cause quality accidents in the circulation of medical commodities, so as to prevent quality accidents. In the whole process of production, management and sales of medical commodities, quality problems may occur at any time due to internal and external factors, and strict measures must be taken in all these links to fundamentally ensure the quality of medical commodities.
2. Different publishers:
The publisher of GMP is the World Health Organization; The current GSP is promulgated by the State Administration of Pharmaceutical Products.
/iknow-pic.cdn.bcebos.com/6a600c338744EBF8E92aefd7F9D72a6159a742 "target =" _ blank "title =" "class =" ikqb _ img _ alink ">. /iknow-pic . cdn . BCE Bos . com/6a 600 c 338744 ebf 8d 8 e 92 aefd 7 f 9d 72 a 6 159 a 742？ x-BCE-process = image % 2f resize % 2Cm _ lfit % 2Cw _ 600% 2Ch _ 800% 2c limit _ 1% 2f quality % 2Cq _ 85% 2f format % 2Cf _ auto " esrc = "/ 6a 600 c 338744 ebf 8d 8 e92 aefd 7 F9 d 72 a 6 159 a742 "/>；
Extended data:
According to the relevant requirements of the new GMP, the time for transformation certification of many pharmaceutical manufacturers is tightening.
Among "other drugs", solid preparations account for a considerable part. Commonly used solid dosage forms are powder, granule, tablet, capsule, dripping pill, film, etc. , accounting for about 70% in pharmaceutical preparations.
Therefore, with the approaching of the deadline of the new GMP certification, the transition period for related enterprises is actually running out. Considering the future development of enterprises and related work and avoiding the problem of "traffic jam" in certification work, many enterprises have advanced the transformation and certification of new GMP to more than half a year, which is also encouraged by relevant departments.
/baike.baidu.com/item/GMP/405 "target =" _ blank "title =" Only one link can be selected to take effect "> Baidu Encyclopedia -GMP
/baike.baidu.com/item/gsp% E8% AE% A4% E8% AF% 81/8358690 # 2 "target =" _ blank "title =" Only one link can be selected to take effect "> Baidu Encyclopedia -GSP.