When: Available on demand. This is a recording of the live webinar which took place in February 2019
Learning objectives
- National requirements for medical devices in Russia
- Product classification criteria
Submission planning/ approval timeline
- Labelling requirements (Languages/ symbol/ other details)
- General regulatory challenges for lifecycle management in Russia
- Key differences between the EU and Russia requirements
Target audience
Regulatory professionals who would like an overview of the regulatory framework for Medical Devices Russia.
Presenter
Angelica Banccanelli -Medical Devices Regulatory & Compliance Consultant, Pharma Quality Europe
CPD
This course offers 1 CPD hour for successful completion, to learn about why CPD is important visit the Lifelong Learning page.
How do I register?
Prices
| Type |
Member |
Non-member |
| Standard |
£70 + VAT |
£95 + VAT |
Discounted Places
A limited number of discounted places are available at the rates below for those:
Please email meetings@topra.org for a discount code before making your booking.
| Type |
Member |
Non-member |
| Discount |
£35 + VAT* |
£47.50 + VAT* |
* VAT, if applicable, is charged at a rate of 20%.
Terms and conditions
Please read the training terms and conditions before booking this webinar. By booking this webinar, you are agreeing to the terms and conditions.