NSF Health Sciences

Experts in Medical Device Training, Testing, Consulting, Auditing and Regulatory Support

EU Medical Device Regulations: Are You Ready for the Impact?

NSF Health Sciences

Establishing in-vitro diagnostic products and medical devices in Europe may mean making changes to your business beyond comprehension of new regulatory requirements.

These changes will affect many assumptions made within your business planning activities.

At NSF, we understand the medical device business, especially the strategic planning processes employed to achieve both regulatory compliance and shareholder value. NSF understands that if you underestimate the impact of these new regulations then your company's business results will be at risk.

To aid you, NSF experts have prepared a simple 5 step process to understand the business impact to both products already on the market and new product introductions in Europe. These steps form part of the NSF EU Medical Device PORTFOLIO assessment consulting service.

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