Skip to content
Contact an Expert

Webinar: Medical Device Market Access FAQ

View On Demand Session

Duration: 60min

Language: English

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.

View On Demand Session

Contact Standards Research

Are you interested in learning more about our research? Email us at [email protected].

Join the Research Community

Join the CSA Community today so you can keep informed about research that is critical to standards development

When you join the CSA Community, you’ll gain access to the CSA Group Research Space. You can learn about current studies, get the latest information on upcoming programs, ask questions, andget involved in future research.

Contact an

We’re always here to help. Let’s talk.

We’re here to answer your questions and help you get started right away. Call or send us a message anytime.

Contact Us