🇨🇿 Basics of Regulation of Medical Devices Simply

The event is held in Czech language only!

Do you find the regulation of medical devices too complex to understand quickly? Do you have a problem with the fact that most training events require participants to already have a basic knowledge of the subject and focus on superstructural areas? Do you think it would be nice to have someone explain the complete basics in a semi-sopathic way? If you answer yes to any of the above questions, then this online seminar is for you. We will try to explain the basic concepts and processes in an easy-to-understand way. We will walk participants through the entire life cycle of a medical device from initial idea to disposal.

Lecturers:

• Jakub Král
• Barbora Charvátová

Content:

• brief overview of legislation
• tips on appropriate sources of information
• key institutions and their tasks
• introduction to the most important concepts
• an overview of the main processes and their interrelationships
• specific sub-areas of regulation (production, distribution, use, reimbursement, advertising, …)
• key regulatory documents
• the most important obligations of manufacturers, importers and distributors
• responsibilities of health service providers

Additional information:

• During the webinar, participants will have the opportunity to ask questions
• each participant will receive a certificate of participation
• a PDF presentation will be sent to all participants

Participation fee:

• 3.900 CZK excluding VAT
• 100% cancellation fee applies after bindingly confirmed registration, but with the possibility of sending a replacement participant