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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.
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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.
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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.
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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.

EastPoint Innovation Successfully Obtains International AAALAC Accreditation!

2025年06月16日

Recently,  EastPoint (Hangzhou) Innovation Co., Ltd. officially obtained the AAALAC International FULL ACCREDITATION.  This accreditation affirms the company's outstanding performance in experimental animal work.  It demonstrates that EastPoint Innovation has reached international standards in animal breeding management,  welfare protection,  research quality,   personnel training,   facility compliance,  etc.


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AAALAC International is a global authoritative certification body for laboratory animal management.  The evaluation covers:  animal housing environments,  facility conditions,  professional staff operations,  animal welfare,  and ethical review of experimental protocols.  EastPoint Innovation has successfully obtained this honor.   This demonstrates the company’s long term commitment on animal management.  It is an important milestone in practicing the philosophy of "respecting science, revering life, and pursuing excellence".

EastPoint Innovation will take this accreditation as a starting point and uphold the core spirit of AAALAC.  The company will manage animals testing with global standards and provide quality services for medical device innovations.


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