Sustainability FAQ
Why is sustainability important in medical device development and manufacturing?
What impact does it have? What is important to consider?
Read for the answers…
Sustainability
EU MDR Requirements for Implant Cards
EU MDR requires manufacturers to provide “implant cards” for patients with implanted medical devices. The intention is to make crucial information about implants easily accessible to patients. CLIN-r+ explains what manufacturers are responsible for.
Quality Management System (QMS)
A Medical Device Quality Management System (QMS) is a set of policies, processes, and procedures that a medical device manufacturer uses to ensure that their products are safe and effective for their intended use. CLIN-r+ explains what it is, and why it’s so important for manufacturers.
Sustainability Assessments – Future Impact on Medical Device QMS
The WHO vision for an environmentally sustainable health system is one that improves, maintains, or restores health, while minimizing negative impacts on the environment and leveraging opportunities to restore and improve it, to the benefit of the health and well-being of current and future generations. CLIN-r+ looks into sustainability assessment and what this means for manufacturers.
Sustainability Assessments – Future Impact on Medical Device QMS Read More »
Medical Device Sustainability
Sustainability is a pressing matter that medical device developers and manufacturers need to embrace, but it is not straightforward. This paper looks at where we are now, and what it means for manufacturers and the design of their medical devices.
