JAN 8, 2020: 13:00-14:00 PM CET / 12:00-13:00 PM GMT
Mandatory webinar: Information regarding Mölnlycke Health Care product transfer to EU Medical Device Regulation (MDR).
Since September 2016, Mölnlycke Health Care AB has been working on an MDR compliance program. The purpose of this program is to secure compliance with the obligations under EU Medical Device Regulation 2017/745 (MDR).
In this webinar we will address how the MDR transfer of products will affect local markets. Therefore please make this meeting a priority.
This webinar is mandatory for General Managers, Marketing Directors and Marketing Managers, local Product Manager/s, Clinical Director/s and Manager/s, Regulatory Director/s and Manager/s, Legal Director/s and Manager/s.
The webinar will be followed up by Q&A Skype-meetings during Jan-Feb 2020.
For those not able to attend, an on-demand webinar will be accessible by using the same registration link, as of Jan 8, 15:00 CET.
The iLearn course MDR – Medical Device Regulation i is mandatory. Please complete by Jan 31st, 2020.
• Introduction (Cathy Dalene, EVP Wound Care Franchise and Global Marketing)
• About MDR and Article 7 (Christina Lewing, Global RA Director)
• MDR and implications for local markets