Without it, manufacturers face risks of recalls, compliance issues, and lower productivity
Understanding the standard is essential
The FDA’s new QMSR will harmonize with ISO 13485 for medical device quality management
An excellent technological tool that improves quality and compliance
Amid rising prices, medical device supply chains need greater scrutiny and standardization
Findings point to faster way to find bacteria in food, water, and clinical samples
Take this opportunity to prepare for the future
QMSR for medical device companies
CAPA systems require continuous management, effectiveness checks, and support
The answers will reveal the truth about your product and get it to market faster
Automation maintains a living document and integrates risk management
The benefits of AI in healthcare have been identified by many global regulators
Whatever you eat, NIST is working to keep it safe
Don’t wait until something bad happens to make a change
A lack of integration hampers quality compliance across a product’s life cycle
A well-defined CAPA program is a framework for quality and effectiveness
IAF CertSearch now mandatory for accredited certification bodies
What’s the difference?
How to ensure the integration of IoMT devices in your practice
Options to address the risk of combustible dust explosions for NFPA 61 compliance