Rachel Hardy Prado's Location
Paris, FR
Rachel Hardy Prado's Work
- Evaluateur - Technical reviewer @ GMED
- Strategic Regulatory Consultant - Medical Device European Regulation @ MedPass International
- Medical devices project manager - Product reviewer - Site auditor at the french notified body G-Med @ LNE
- Quality manager and regulatory affairs manager @ OBL
- Ingeneer In LEMI @ LEMI Laboratoire de Toxicologie et Ingénierie cellulaire et tissulaire
Rachel Hardy Prado's Education
- Université de Bordeaux 1 et 2
Master Medical devices (nouvellement BIDIM) (Matériaux pour le vivant)
1999 - 2000 - Université d’Orléans
Maîtrise (Biologie cellulaire et moléculaire)
1995 - 1999
Rachel Hardy Prado's Skills
- Medical Device Directive
- ISO 13485
- Iso 13485 Cmdcas
- ISO 14971
- ISO 9001
- Conception de produit
- Iso 15378
- Jpal
- Microbiology
- Biocompatibility
Rachel Hardy Prado's Summary
Rachel Hardy Prado, based in Paris, FR, is currently a Evaluateur - Technical reviewer at GMED, bringing experience from previous roles at MedPass International, LNE, OBL and LEMI Laboratoire de Toxicologie et Ingénierie cellulaire et tissulaire. Rachel Hardy Prado holds a 1999 - 2000 Master Medical devices (nouvellement BIDIM) in Matériaux pour le vivant @ Université de Bordeaux 1 et 2. With a robust skill set that includes Medical Device Directive, ISO 13485, Iso 13485 Cmdcas, ISO 14971, ISO 9001 and more, Rachel Hardy Prado contributes valuable insights to the industry. Rachel Hardy Prado has 1 email on RocketReach.
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