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Recent Posts
- 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...
- Generis
- March 16, 2016
Operational excellence is a key area of focus at the American Biomanufacturing Summit taking place on May 10-11 in San...
- Generis
- March 15, 2016
We were thrilled that Robert Sparadoski, Associate Vice President, Quality Assurance at Ferring Pharmaceuticals could...
- Generis
- March 14, 2016
There are many changes on the horizon for the life sciences industry. To help pharmaceutical manufacturers navigate the...
- Generis
- March 14, 2016
Medical device developers must take into account numerous safety, quality and risk factors to ensure the durability and...
- Generis
- March 11, 2016
Quality management is a key focus at the American Biomanufacturing Summit 2016. Manufacturers are facing increased...
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