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Recent Posts
- Generis
- September 27, 2016
A validated sterilization cycle is a requirement for many medical devices, and the appropriate sterilization method...
- Generis
- September 27, 2016
In today’s environment of strict regulation and reduction in spending for healthcare, life sciences companies are under...
- Generis
- September 26, 2016
Medical device organizations face a number of regulatory and compliance challenges ranging from design and development...
- Generis
- September 22, 2016
With the American Medical Device Summit 2016 right around the corner we wanted to take some time to sit down with...
- Generis
- September 21, 2016
Medical device developers face an array of regulatory, compliance, quality and risk challenges. Throughout the past...
- Generis
- September 19, 2016
Computer-aided design (CAD) is an industrial art that results in lower product development costs and greatly shortened...
- Generis
- September 15, 2016
Surface preparation is a critical manufacturing process that enables sealing, bonding, painting, coating, printing and...
- Generis
- September 12, 2016
In our previous posts we have looked into some of the challenges that documentation can present during a medical...
- Generis
- September 8, 2016
The American Medical Device Summit is less than one month away! The summit will draw on the knowledge of over 40...
- Generis
- August 31, 2016
Managing costs throughout the product life cycle is critical to a company’s long term viability and profitability....
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