0571-26280011

epi@eastpoint.com.cn

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About Us
Drawing on the unique characteristics of our customers' medical device products, we offer a tailored and personalized integrated service model that spans from preclinical to clinical research and registration consultation. Our aim is to provide comprehensive support throughout the product development lifecycle, ensuring the delivery of essential preclinical research data, conducting rigorous clinical research, and facilitating seamless registration declaration processes.
Business
Drawing on the unique characteristics of our customers' medical device products, we offer a tailored and personalized integrated service model that spans from preclinical to clinical research and registration consultation. Our aim is to provide comprehensive support throughout the product development lifecycle, ensuring the delivery of essential preclinical research data, conducting rigorous clinical research, and facilitating seamless registration declaration processes.
Business Acceptance

Business Acceptance

Drawing on the unique characteristics of our customers' medical device products, we offer a tailored and personalized integrated service model that spans from preclinical to clinical research and registration consultation. Our aim is to provide comprehensive support throughout the product development lifecycle, ensuring the delivery of essential preclinical research data, conducting rigorous clinical research.
News Center
To best serve our customers' needs, we offer a personalized integrated service model tailored to the characteristics of their medical device products. This model encompasses a comprehensive range of services from preclinical to clinical research and registration consultation, ensuring the provision of essential preclinical research data, conducting robust clinical research, and facilitating seamless registration declaration processes.
Team Introduction
Based on the unique features of the customer's medical device products, we tailor a personalized integrated service model spanning from preclinical to clinical research and registration consultation. This enables us to better assist customers by providing comprehensive support, including basic preclinical research data, clinical research, and assistance with registration declaration for the product.

Testing service flowchart (including biological evaluation testing, chemical analysis, and other research content)

2024年02月27日

Detection service flowchart

检测服务流程图.png


Instructions for filling out the commission form

To ensure a smooth and accurate process during the completion of the contract commission form for inspections, please take note of the following guidelines:

1. **Sample Labeling**:  
  - Each sample or group should be clearly labeled with essential information such as the sample name, model specifications, production batch number, production unit, and any other relevant details.  
  2. **Consistency Check**:  
  - The sample information provided in the contract commission form must match exactly with the details presented on the sample labels attached to the samples.  
3. **Method Statement Requirement**:  
  - For biological testing of medical devices, a detailed method statement outlining the testing procedures should be included.  
4. **Document Duplication**:  
  - All accompanying materials must be duplicated and officially stamped with the commissioning unit's official seal or contract seal.  
5. **Mailing Information**:  
  - The designated mailing address for both the samples and related information is East Point Medical.

By adhering to these guidelines, you can help ensure the efficiency and accuracy of the inspection process while minimizing the risk of errors and misunderstandings.