Maud Humbert's Location
Lyon, FR
Maud Humbert's Work
- Senior Manager Regulatory Affairs @ Baxter International Inc.
- Regulatory Affairs Consultant @ Baxter International Inc.
- Director QA and RA @ DEDIENNE SANTE
- Regulatory,Quality and Supply Chain Manager @ Stryker
- Regulatory, Quality and Supply Chain Manager @ Small Bone Innovations, Inc.
- QA Specialist @ Abbott Ireland Diagnostic Division
Maud Humbert's Education
- Polytech Lyon
Master's Degree (M2) (Medical Device Regulatory and technical Affairs)
2015 - 2016 - Université de Nantes
University degree (DEUP) (Chemistry / Biology)
1993 - 1994 - Lycée de la Plaine de l'Ain - Ambérieu
Technical degree (BTS) (Biochemistry / Biological Engineering)
1991 - 1993
Maud Humbert's Skills
- Medical device
- CE marking approval
- MDD 93/42/CE
- MDD 2007/47/CE
- IVD 98/79/CE
- ISO 13485
- 510(k) clearances
- FDA 21 CFR
- Regulatory submissions
- Fluent in english
Maud Humbert's Summary
Maud Humbert, based in Lyon, FR, is currently a Senior Manager Regulatory Affairs at Baxter International Inc., bringing experience from previous roles at Baxter International Inc., DEDIENNE SANTE, Stryker and Small Bone Innovations International. Maud Humbert holds a 2015 - 2016 Master's Degree (M2) in Medical Device Regulatory and technical Affairs @ Polytech Lyon. With a robust skill set that includes Medical device, CE marking approval, MDD 93/42/CE, MDD 2007/47/CE, IVD 98/79/CE and more, Maud Humbert contributes valuable insights to the industry. Maud Humbert has 1 email on RocketReach.
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