Department Introduction

Biomaterials Translational Research Center | Our Speciality

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Excellence

(A).Biocompatibility testing

In 1992, the International Organization for Standardization published ISO 10993 as the basis for the biological assessment of medical apparatus. As the biomedical market is booming, the center provides experimental services in line with ISO 10993 to assist products in preclinical safety testing.


Service items include :

A1. Cytotoxicity tests A2. Irritation tests (animals) A3. Sensitization tests (animals)

A4. Genotoxicity tests A5. Blood compatibility A6. Heat source test (animals)

A7. Systemic toxicity test (animals) A8. Implantation tests (animals)

(B). New product development testing

R&D is the key to corporate sustainability. The center provides new product development test services in line with the ISO 17025 management system to increase the industry's competitiveness.

The range of services covers:

B1. Development of orthopedic and dental materials B2. Development of health foods B3. Research and development of stem cells

B4. Development of medical materials products B5. Development of dressings B6. Others

(C). Effect confirmation testing

The center abides by relevant regulations, provides product validation services, and conducts rigorous scientific verification by professional research teams, so as to help improve product value and safety.

The range of services covers:

C1. General cell experiments C2. Cell differentiation experiments C3. Animal implantation experiments

C4. Mechanical tests C5. Fluorescent image shooting C6. Medical image shooting

C7. Electron Microscopy shooting C8. Tissue sections and staining C9. Others

(D).Custom-made commissioned testing

The center is comprised of researchers and physicians in various fields, which can provide a variety of experimental services. In the case of special experimental purposes, a custom-made commissioned test can be carried out. In the event of animal trial or clinical trial needs, a technical operation can be performed after the review of the submitted animal trial protocol or clinical trial protocol.

 

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