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Recent Posts
- Generis
- August 29, 2016
Medical device developers are evolving and introducing new products and variants into the market. With this evolution...
- Generis
- August 17, 2016
Deciding on the appropriate region for your manufacturing operations is a vital step. Many US manufacturers consider...
- Generis
- August 16, 2016
You may be familiar with how 5S Programs, Kanban Systems and Kaizan Events help drive your lean manufacturing...
- Generis
- July 25, 2016
Wearable devices have become a commodity; devices act as fitness and health trackers, work and lifestyle guides as well...
- Generis
- July 15, 2016
Setting up manufacturing operations in Mexico requires an initial assessment of the appropriate legal entity framework;...
- Generis
- July 6, 2016
Automotive consumers are demanding, and are placing OEMs under increased pressure to provide enhanced value through the...
- Generis
- July 5, 2016
There has been a great amount of discussion around the impact that UDIs will have on medical device developers,...
- Generis
- June 30, 2016
In August 2015 the FDA’s Center for Devices and Radiological Health (CDRH) implemented a requirement for manufacturers...
- Generis
- June 21, 2016
Quality control and regulatory compliance are paramount in medical device development. A fully validated tool can help...
- Generis
- June 14, 2016
The evolving regulatory landscape and the accelerated pace of medical device innovation are increasing pressure on...
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