Dear audience of the RAPS regulatory open forum:
I am Susan Pérez, master student at the Turku University of Applied Science, Turku- Finland.
My thesis topic focuses on " what are the implications of the IVDR ( in vitro diagnostic medical device regulation; EU/2017/746) and MDR ( medical device regualtion; EU/2017/745) on the business and its management".
Please, find enclosed a list of questions which aim at collecting opinions from manufacturers, researchers, consultants. You do not need to fill every question but I would feel very thankful if you could provide as much information as possible. Also, you do not need to write the company name if you wish to keep it confidential but instead describe the company number of employees.
I know you all have tight schedules and I would appreciate it a lot if you could make time to help me.
Please,
send the completed questionnaire (attached) to perez.susan.fi@gmail.com.------------------------------
Susan Karen Perez Gamarra
Student
TUAS
Turku
Finland
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