The manufacturing of medical devices is a highly complex and highly regulated industry that is continually changing. Rapid advances in technology introduces manufacturing challenges, requiring companies to be more diligent in production and compliance to ensure that the product performs as intended each time. Our new handbook explores the challenges and trends impacting medical device manufacturing, reviews core regulations, and discusses how monitoring can help your company address compliance challenges, stay audit-ready and protect patients. You’ll learn everything you need to know about what’s changing in the medical device industry and how environmental monitoring can help you stay protected:

• Trends and challenges driving medical device development
• Major device categorizations and regulations governing the industry
• The impact of emerging technologies on patient care
• How to address compliance challenges and prepare for audits
• The benefits of environmental monitoring

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