中国注册(NMPA)

中国注册  

China NMPA Registration and Marketing  


BAO Pharma is your preferred Partner to increase your business and presence into selected markets by providing a full pack of services through its Wider China Marketing Network.


Our deep knowledge, experienced Regulatory Team and local presence allow us to have access to China markets, one of the largest pharmaceutical markets especially China Launching Project of Quality Consistency Evaluation of Generics. 


More APIs, excipients Manufacturers are Welcome.

原辅料注册和销售

公司与印度原辅料生产商、批发商,建立良好的合作关系,多赢的合作理念和开放的多种方式的合作模式。目前业务主要是注册和代理销售 引进印度、意大利、西班牙、瑞典原料药,以及出口原料药、中间体。


制剂注册和销售

中国实施的《关于在公立医疗机构药品采购中推行“两票制”的实施意见》,《联盟地区药品集中采购文件》(4+7集中采购)及变更齐全到可能的全国集中采购,深刻影响中国 公司利用着力引进有一定难度的制剂或者联合开发新制剂。,利用公司在临床、销售渠道的优势,为中国消费者带来福祉。同时也提供多种模式的技术转让服务

制剂的合作模式:技术购买,技术转让,联合开发,知识产权+CRO+仿制药生产商的 多种合作模式。


Finished Dosage Registration and Marketing.

As per China policy like Centralized Procurement and Procurement with target quantity, have made great changes on sales system of Formulation in China. BAO Pharma will introduce some difficulty or innovator drugs to China Markets. We have our own clinical facilities and regulatory team. Technology transfer is also fine.


Multi-Win Philosophy and Open-minded for Multi-dimensional Collaborations.

Technology Acquisition  

Technology Transfer     

Joint Development      

IP+CRO+Sponsor    


 医疗器械注册和销售

 BAO Pharma have over 6 years experience in distributing and marketing of medical devices in China. We also provides specialized product registration services for China and Overseas manufacturers. 

Main Laws and Regulations:

1.   Regulations on the Supervision and Administration of Medical Devices (State Council Decree No. 680 in2017) promulgated on May 4, 2017

2.   Provisions on Medical Device Registration (CFDA Order No. 4 in 2014) promulgated on July 30, 2014

3.   Provisions on Registration of IVD Reagents (CFDA Order No. 5 in 2014) promulgated on July 30, 2014

More Medical Device Manufacturers are welcome.

本公司代理欧美日多家企业的医疗器械,涵盖三类医疗器械,为国内客户提供专业的技术服务和解决方案。熟悉进口《医疗器械监督管理条例》注册及进口相关流程。目前已经进口第一、第二、第三医疗器械代理清关一整套服务。参与国际重点实验室、医疗机构项目的招投标,并与供应商、客户建立良好的合作关系。

同时,也出口国内的医疗器械到中东非洲东南亚国家和地区。


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