Nadine Duplay
Regulatory Affairs Manager with 9 year experience in Medical Devices (from Class I to Class III) and In... | Switzerland
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Nadine Duplay’s Emails nd****@ha****.com
Nadine Duplay’s Phone Numbers No phone number available.
Social Media
Nadine Duplay’s Location Switzerland
Nadine Duplay’s Expertise Regulatory Affairs Manager with 9 year experience in Medical Devices (from Class I to Class III) and In Vitro Medical Devices. In charge of MDR technical files (initial submissions to NB, responding to deficiency reports, maintenance), leading a team of consultants. Also responsible for international registrations (EU, Middle-East & Africa), Product Development & Change Management, Field Safety Corrective Actions, Internal & External audits.
Nadine Duplay’s Current Industry Haemonetics
Nadine
Duplay’s Prior Industry
Epfl
|
Igem Competition
|
Novartis
|
Anteis
|
Haemonetics
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Work Experience
Haemonetics
Regulatory Affairs Manager
Thu Jun 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Haemonetics
Senior Regulatory Affairs Specialist
Tue Jan 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Jul 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
Haemonetics
Regulatory Affairs Specialist
Sat Nov 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Dec 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Anteis
Regulatory Affairs Coordinator
Fri Nov 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Oct 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Anteis
Regulatory Affairs Intern
Sat Jun 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Oct 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)
Epfl
Research assistant
Sun Jul 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Sep 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)
Novartis
International BioCamp 2011 Alumni
Mon Aug 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Aug 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time)
Igem Competition
Team member
Tue Feb 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Nov 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time)
Epfl
Research assistant
Fri Oct 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Jul 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Nadine Duplay Email Addresses
FAQ About Nadine Duplay
-
Nadine Duplay is located at
Switzerland -
Nadine Duplay is a
Regulatory Affairs Manager with 9 year experience in Medical Devices (from Class I to Class III) and In Vitro Medical Devices. In charge of MDR technical files (initial submissions to NB, responding to deficiency reports, maintenance), leading a team of consultants. Also responsible for international registrations (EU, Middle-East & Africa), Product Development & Change Management, Field Safety Corrective Actions, Internal & External audits. Haemonetics -
Nadine Duplay currently works in the
Haemonetics -
Nadine Duplay specializes in
Regulatory Affairs Manager with 9 year experience in Medical Devices (from Class I to Class III) and In Vitro Medical Devices. In charge of MDR technical files (initial submissions to NB, responding to deficiency reports, maintenance), leading a team of consultants. Also responsible for international registrations (EU, Middle-East & Africa), Product Development & Change Management, Field Safety Corrective Actions, Internal & External audits. -
Nadine Duplay speaks the following languages:
No languages available. -
Nadine Duplay has prior experience in the following industries:
Haemonetics , Haemonetics , Anteis , Anteis , Epfl , Novartis , Igem Competition , Epfl -
Nadine Duplay has the following professional experience:
Haemonetics , Haemonetics , Haemonetics , Anteis , Anteis , Epfl , Novartis , Igem Competition , Epfl . -
You can view Nadine Duplay’s
LinkedIn profile at LinkedIn URL. -
Nadine Duplay’s work email addresses are
[email protected] . -
Nadine Duplay works at
Haemonetics
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