As science and technology progresses, Medical Devices are becoming increasingly sophisticated and innovative and therefore regulatory requirements evolve accordingly to ensure the safety of products and users both in Europe and elsewhere. Therefore, manufacturers, assemblers, sterilizers, distributors and importers of medical devices must comply with the regulatory requirements where they will manufacture and/or market their products.
In Azierta we are leaders in support and consultancy in medical devices regulation and we can help you to get your products on the market, evaluate to what extent the regulatory changes affect you and adapt your products to the applicable regulatory requirements.
