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Recent Posts
- Generis
- May 2, 2016
Successful serialization strategies require a global approach and considerations regarding installation and aggregation...
- Generis
- April 28, 2016
In the build up to the American Biomanufacturing Summit, we sat down with James Klingelhoefer, Regional Sales Director...
- Generis
- April 27, 2016
dMedical device manufacturers are facing increasing challenges in the development, production and commercialization of...
- Generis
- April 27, 2016
Medical device developers have a series of hurdles they need to navigate in order to successfully bring their device to...
- Generis
- April 25, 2016
In today’s post we draw on the expertise and insights of EngiSystems to examine the growing impact of recalls in the...
- Generis
- April 14, 2016
At the American Biomanufacturing Summit last May we had the opportunity to sit down with one of our key speakers,...
- Generis
- April 11, 2016
Regulatory bodies such as the FDA require medical device manufacturers to document and track huge amounts of...
- Generis
- March 28, 2016
“When granting regulatory approvals for medical devices, both IEC 62366 and the FDA have emphasized the importance of...
- Generis
- March 22, 2016
eBook: Q&A with Brandon Varnau, Vice President and Head of Operations Quality, Sanofi Specialty Care
Our next eBook features industry insights and forecasts from Brandon Varnau, Vice President and Head of Operations...
- Generis
- March 18, 2016
In today’s infographic we take a closer look at the guiding principles of a quality management system (QMS). The goal...
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