Personal Information
Entreprise/Lieu de travail
Zürich Area, Switzerland Switzerland
Profession
Regulatory Affairs Manager at Roche Diagnostics
À propos
Highly motivated, dynamic and experienced Regulatory Affairs Manager with excellent communication skills. Experienced in many different areas of Medical Device (including implants) and IVD technology and deep knowledge of aspects such as project management, product development & launch processes, change management, risk management, SW development and Usability.
High personal and professional integrity, able to relate to and create trust in people. Dependable and reliable in supporting team effort, confident and persuasive, able to motivate and communicate.
Strong negotiations skills, ability to manage by influencing, convincing and conducting meetings at all levels.
- Présentations
- Documents
- Infographies
Use of left over samples under the IVDR and GDPR
Erik Vollebregt
•
il y a 6 ans
Regulation of Economic Operators under the MDR and IVDR
Erik Vollebregt
•
il y a 6 ans
Kazakhstan: What information is mandatory on medical device label?
Alexey Stepanov
•
il y a 9 ans
Medical Device Labeling in Russia
Alexey Stepanov
•
il y a 8 ans
FDA Expectations for Traceability in Device & Diagnostic Design
Seapine Software
•
il y a 12 ans
Trends in EU regulation of software as medical device
Erik Vollebregt
•
il y a 6 ans
Becoming more efficient
Dalibor Sever
•
il y a 8 ans
mHealth Israel_Digital Health_The Regulatory Landscape 2017
Levi Shapiro
•
il y a 7 ans
EU cybersecurity requirements under current and future medical devices regulation
Erik Vollebregt
•
il y a 7 ans
New EU Legislation on Medical Devices By G. Bos - BSI (Qserve Conference 2013)
qserveconference2013
•
il y a 10 ans
Travel Tips Learned from Japan! - #japan #traveltips
Empowered Presentations
•
il y a 11 ans