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

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    Quote and Ordar

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    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.

2021保健營養食品拓銷實務研討會

「開創後疫情時代保健營養食品產業新藍海
-保健營養食品國內外法規管理現況及行銷佈局」

 

壹、緣起:

一、目的: 

新冠肺炎疫情自2019年底爆發以來肆虐全球,疫情對於全球經濟帶來衝擊,亦改變消費者行為模式,在此變局下,國內保健營養食品業者更應思考後疫情時代國內外市場如何行銷佈局。 

本研討會聚焦於國內及東協外銷目標市場保健營養食品相關法規管理現況及市場趨勢之探討,內容包括國內食品廣告管理法規、目標市場法規管理制度、國內外市場脈動及行銷推廣實務等。同時因應後疫情時代網路宅經濟商機崛起,探討保健營養食品電視購物、電商通路等虛擬通路之佈局,協助國內保健營養食品業者趁早佈建國內外虛擬通路,開拓新市場。 

二、依據: 

依據經濟部工業局 110年度「保健營養食品產業鏈優化及品質提升」計畫之「保健營養食品產業環境優化暨國際拓銷推廣」辦理保健營養食品拓銷實務研討會。

 

貳、參加對象及人數

食品及保健營養食品相關業者,預計150人。

 

叁、研討會舉行時間:

110年11月11日(星期四)

肆、地點:

線上視訊研討會(請所有參加者使用內建或外麥克風之電子設備參與會議)

伍、報名時間:

即日起至 110年10月29日,或額滿為止。

陸、報名費用:

每人500元整。

柒、報名方式:

一律採網路報名,報名網址如下

http://www.idbevent.org.tw/Events/event_more?id=a90cd1220a9148a9bd22722ed785c367

捌、辦理方式:

因防疫考量,本研討會以線上視訊會議型式辦理。

玖、主辦單位:

經濟部工業局

拾、執行單位:

中華穀類食品工業技術研究所

拾壹、協辦單位:

台灣保健食品學會、台灣保健營養食品工業同業公會


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