International Medical Devices companies

Postgraduate> Master in Business Technology and Health Products *

Master in Business Technology and Health Products *

  • Type graduate

    Master's Degree (official)
  • Area

    Pharmaceuticals and Biotechnology
  • Duration

    60 credits in November 2013 to October 2014
  • Mode

  • Schedule

    Monday to Friday from 16.00 to 20.00 h
  • Language

  • Campus

    The moral (Madrid)

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Technology Sector and Healthcare Products (TPS) is one of the cornerstones of the health system, having experienced dramatic progress in recent decades that have contributed decisively to the extension and improvement of quality of life. This sector includes all companies that produce and supply health products and drugs that are not from a plaster to products as complex as an implantable pacemaker or an MRI.


Health is an inalienable right and therefore health benefits and industry in support of the same, continue to grow despite the economic crisis. Likewise, innovation by incorporating new technologies and materials is necessary to have professionals with a is an initiative to provide comprehensive training for graduates who want to acquire knowledge and skills to develop your career in a sector highly attractive.

Although they are very numerous training initiatives within the sector of TPS, never before had made the effort to transfer to an official Master the knowledge and skills that make up a full training proposal for future managers in the industry.

The objectives of the master are:

  1. Fully aware of the TPS sector and businesses that form: with a cloister formed by industry professionals, students know first hand the leading companies in this field.
  2. Know the legal and regulatory environment: essential to work in an industry with very specific legislation.
  3. Developing skills both from the standpoint of academic and business: enabling rapid integration, productivity and opportunities for professional growth and development.

The lectures are supplemented by lectures, scheduled visits, and educational activities that aim to maximize the interaction with the student.

The agreement between the Federation and the European University Business sector (FENIN), which represents more than 550 national and international companies, guarantees the performance of paid to all students in the associated companies. Highlights include:

2004-05-06 14:36:24 by eyt_sf

How to get an international job in SF

Hi. I'm looking for a new job, and would appreciate any help/advice you could give me on the topic.
-BA in an Ivy league Japanese university (2000)
-1yr and a half exp. sales in medical devices (Japan)
-1yr exp. in medical program coordination (SF).
-Fluent in Japanese and English
OK. Here is my ideal job. I would like to work for an American company with a Japanese branch, and would like to introduce/educate new products to the Japanese branch. Or a position where I could communicate beween the Japanese and American companies, and travel overseas

2007-12-21 20:59:31 by shakesfear

Copy and Paste time!!! :)

In 1989, the Japanese government funded the Laboratory for International Fuzzy Engineering Research with an advance of some $35 million and more than 40 member firms. Japanese cars are starting to use fuzzy transmissions. In 1989, Honda awarded its prestigious Honda prize to Zadeh for his contributions to Japanese technology. U.S. companies have been extremely reluctant to jump on the fuzzy bandwagon. Exceptions are Rockwell, which markets several fuzzy devices; Otis Elevator; and General Motors, which uses fuzzy logic in the transmission of its Saturn car.
Bart Kosko, author of Fuzzy Thinking, is the movement's most controversial and combative promoter

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  • Avatar Strattus 13 Anyone knows whats the basic functions of a International regulatory specialist?
    Jan 22, 2013 by Strattus 13 | Posted in Other - Business & Finance

    I have been offered a position at a medical devices company as an International Regulatory Specialist. They don t necessarily ask for experience, so I was wondering if anyone can give me some insights about this position. What are the main duties, and is all of the job paperwork (as one of my friend s put it). Thank you very much

    • Try this on for size: PURPOSE OF JOB: Main areas of responsibility are to provide direct support to the regulatory department and to maintain auditable regulatory files and correspondence ensuring compliance with FDA and international regulations and guidelines. Responsible for coordinating efforts associated with the preparation of regulatory documents or submissions including establishing and tracking regulatory project timelines, status and documents. MAJOR DUTIES AND RESPONSIBILITIES: • Responsible for assisting with the coordination and preparation of regulatory submissions (510(k) …