Webinar: Medical Device Market Access FAQ
Cost: Free of charge
Target Group: Product development professionals, quality managers, R&D professionals, design and compliance engineers and regulatory affairs professionals from medical equipment manufacturers.
Content: The requirements for medical device market access can be complicated. There are various regulations, directives and standards that medical devices must comply with before they can be sold on the market, which vary from market to market. Further, a number of these documents have recently been revised, or are due to go through transition. Quality and regulatory affairs teams must therefore ensure that they fully understand the intricacies of these requirements to ensure on-going compliance.
This webinar will provide answers to the most frequently asked questions during the market access and approval process of electro-medical devices. You will also get the chance to ask individual questions relevant to your specific product.
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