About
MDG

Medgaea Life Sciences is a third party laboratory that is certificated for OECD GLP, TFDA GLP, ISO 17025 and ISO 9001. Maily based on preclinical CRO, we provide total-soltion services to assist biotechnology industries successfully obtain the product certification and exploit internation market.

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CRO

  • check

    Needs Discuss

  • check

    Quote and Ordar

  • check

    Timetable Schedule

  • check

    Report Launch

  • done

    Case Closed

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Services

With devoting to our core value 『Honesty•Accuracy•Professionalism•Responsibility』,

We have successfully assisted our customers to successfully obtain the product certification in FDA, CE, TFDA and NMPA.

Medical Devices

One of the first priority of medical devices R&D is their safety. The Biocompatibility test is mainly followed the ISO 10993 international standard.

Cell therapy and Regenerative medicine

We assist the safety, effectiveness tests during the R&D process of cell therapy product. All the tests are complied with GLP.

Pharmaceutical development

As the agent of SNBL in Taiwan, will help new drugs company to complete non-clinical trials in medium, large animals and primates in the research and development stage.

Agrochemical and Enviromental Agents

The agroculture products need to review their toxicological data in advance, and all the tests must be carried out in complies with GLP.

Chemical Substances

Providing the toxicological test information!
EPA acquired the test information as the core basis to evaluate the substance announcement.

Health Food/ Ingredients

Provide safety, efficacy and stability tests for food ingredients and health foods.

Registration

Provide registration services.

Pharmaceuticals

Provide batch examine for medicine release, including pyrogen, acute systemic toxicity and other tests.

Laboratory animals and Equipment

An agent and supplier based on research and development of animal experiments, providing import services for various disease model animals in research institutions.

| 發布日期:2025-02-19 | 更新日期:2025-02-19

 

主旨:

 

公告114年度國產維生素類錠狀膠囊狀食品查驗登記業務委託「財團法人台灣食品產業策進會」審查。

 

依據:

 

食品安全衛生管理法第21條第6項及食品與相關產品查驗登記業務委託辦法第9條。

 

公告事項:

 

一、旨揭業務之受託機構名稱、所在地、執行業務種類及項目與委託期限詳述如下:

(一)受託機構名稱:財團法人台灣食品產業策進會。

(二)所在地:106660 台北市大安區復興南路1段127號14樓。

(三)執行業務種類、項目及範圍:辦理國產維生素類錠狀膠囊狀食品查驗登記之新案、許可文件展延、變更、移轉等業務委託審查。

(四)委託期限:自114年1月1日至114年12月31日。

 

二、經委託之查驗登記申請案件辦理流程,請參考「食品與相關產品查驗登記業務委託辦法」第11條規定。

 

 

檔案下載
食品與相關產品查驗登記業務委託辦法
公告114年委辦執行機構