1. GMP China Ltd. will offer technical validation, preparation for technical documents, inspection and acceptance of export equipments.     For the sake of meeting the requirements of validation in accordance with “GMP”, “FDA, WHO_GMP, EGMP” standard,  GMP
    will convert the relative technical documentation presented by manufacturer into an appropriate file format according with  the     international business tradition qua accessories for the export facilities. At the same time, The Company will provide services such     as technical validation, preparation for technical documents, inspection and acceptance of export equipments to pharmaceutical     machinery manufacturers all nation wide.
2. The company will provide technical services such as calibration of machines;
3. The company will provide consultation services for pharmaceutical machinery and packing machinery, pharmaceutical packing     materials, raw drug materials etc.
4. The company will provide a comprehensive project solution for pharmaceutical engineering.

GMP documentation：
    1、Design Qualification Protocol (DQ)
    2、Report of DQ (DQ)
    3、Installation Qualification (IQ)
    4、Operation Qualification (OQ)
    5、Performance Qualification (PQ)
    6、Production Validation Protocol (PV)
    7、Cleaning In Place
    8、Standard Operation Procedure (SOP)
    9、Factory Acceptance Test (FAT)
    10、Site Acceptance Test (SAT)
    11、Standard Maintenance Procedure (SMP)
    12、Manual