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Recent Posts
For medical device manufacturers across the globe, among their top priorities will inevitably include complaint...
A Frank Discussion on Economic Operators and How Maetrics Can Lead, Guide and Support Compliance Teams Ahead of the...
Significant changes are ahead for medical device manufacturers. The EU’s Medical Device Regulation (EU MDR), which is...
This is an excerpt from an interview Generis Group did with Assent Compliance prior to the American Aerospace & Defense...
HCL hosted a Lunch & Learn Roundtable Discussion at the American Medical Device Summit 2018 last month in Chicago, IL....
Risk is a major focus in most businesses today, regardless of industry. In the past few years, the Life Sciences have...
Quality is a critical concern in life science manufacturing industries, and leaders across life science companies have...
With technology rapidly changing, a global market, and competition around every corner, quality is one of the most...
Is your company prepared for the new EU MDR? Michael Santalucia, Vice President of Global Regulatory Affairs for Terumo...
Quality management is an integral factor in the development, approval, and commercialization of medical devices. With...