Date: Available on demand. (Original presentation date: 11 January 2019)
Learning objectives
To understand:
- Key differences with pharmaceuticals
- Key players: Roles and responsibilities
- Current Directives and Future Regulations
- Availability of devices
- National issues
- Pharmaceuticals with integrated delivery device
- The future
Target audience
- This webinar is for new entrants to the profession, with at least 6 months of regulatory experience
- Those whose regulatory experience is outside the EU
- Professionals working in medicines with no previous medical device regulation exposure who wish to gain an understanding of this area.
Presenter
Margareth Jorvid has over 30 years’ experience in Regulatory Affairs for pharmaceuticals, medical devices and combination products. She has worked at the Medical Products Agency (MPA), as well as in large and small pharmaceutical and device companies such as Roussel Nordiska, Hoechst Marion Roussel (Stockholm and Paris, France), Neopharma and ProstaLund. Since 2006, Margareth has been CEO of Methra Uppsala AB, LSM group, consulting in regulatory affairs and quality assurance for pharmaceuticals and medical devices. She is a Fellow and Honorary Life Member of TOPRA, board member 2002-2011 and TOPRA President 2005-2006.
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.