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Monday, March 24, 2008
 

So You've Decided to Offshore...

Ok, now what? Everyone knows that offshoring is an obvious way for medical device manufacturers to save costs. The cost of labor in developing countries is far less expensive than it is in developed ones.

But if the decision were based only on that factor, every medical device manufacturer would have already moved all manufacturing operations to developing nations. In fact, there are a ton of considerations that must be taken into account if a device firm is going to send manufacturing operations overseas. In MD&DI’s Guide to Outsourcing this month, we help you sort through some of these considerations.

Mario España of ProNicaragua offers some pointers on how to choose an offshore community, especially when it comes to Latin America. He shows you how to spot the most free-trade-friendly countries, the most interested local governments, and the most conducive cultures to draw from. He also suggests questions that you should ask in order to ensure that you get the best possible deal.

Audrey Soon of International Enterprise Singapore shows how the growth of the biomedical sector in Singapore has made it a more attractive option for offshoring. She helps you determine which operations there have the right credentials for manufacturing medical devices to be sold in the developed world.

And, in an
MD&DI Web exclusive, Rick Rogers and Gray McCord discuss some of the reasons why you should outsource to China—and some of the reasons why you should not. They have come up with 10 questions to ask yourself before deciding whether to start a Chinese operation. If you can’t answer “yes” to at least eight of them, China is probably not the best location for your operations.

Deciding to offshore (and where) should be a careful decision, not a reflexive one. This is the kind of information you need to help you make that decision.

Erik Swain
erik.swain@cancom.com 
  

 

 





Web Exclusive
What Your Mother Never Told You About Outsourcing to China
By Rick Rogers and Gray McCord

Thinking about moving your manufacturing to China? It’s not an easy process, so be sure it’s the right decision.

Pumps and Valves
Optimizing Pumps and Valves
By Dan Schimelman
As more devices become portable, smaller diaphragm pumps and solenoid valves are needed.

Sterilization
The Role of Biocides in Medical Devices
By Jeffrey Ellis
To fight a rise in hospital-acquired infections, more medical devices are being developed with antimicrobial features.

Postmarket Surveillance
Strategies After Product Approval
By Erik Swain
Approval isn’t the end—device firms must have a strong postmarket surveillance strategy for their products.

Diagnostics
Exploring Cap Inspection Systems
By Niels Wartenberg
Miniature imagers combine megapixel technology and vision capabilities to create a suitable choice for many designers.

Product Development Insight
The Benefits of Verification and Validation
By Bryan Chojnowski
Software verification and validation activities could bring more value to an organization.

 More from this issue of MD&DI  



 

U.S. GMP Compliance: A Blueprint for Outsourcing
Device companies can develop a GMP strategy that meets FDA requirements and the specific needs of their outsourcing situations.


   


Check Out MD&DI's 
Device Talk 

A neuroscientist is developing a device that would enable some modicum of sight without any involvement from the eyes or optic nerves.

  


Planning For and Mitigating Risk
Standard practices can reduce risk and facilitate continuous improvement.

  


All Eyes on Singapore
Growth in the country’s biomedical sector could mean more opportunities for U.S. device manufacturers.

 

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