About Audeline
French
Native or bilingual
English
Fluent
Experience
- Rath ConsultantFounder & Expert Consultant in Medical DevicesCONSULTING AND AUDITSAugust 2024 - Today (1 year and 10 months)Paris, FranceIndependent consultant, I support MedTech startups, manufacturers, and distributors in the compliance and reimbursement of their medical devices, offering them personalized support aligned with their needs.- CE Marking (EU 2017/745): strategy, technical documentation, support with Notified Bodies- Clinical: strategy, clinical evaluation plan and report, post-market clinical follow-up (PMCF)- Reimbursement: strategy, LPPR, LATM, intra-GHS, transitional, PECAN, innovation gói- Quality: ISO 13485, implementation or improvement, support, audits- Risk management file ISO 14971- Post-market surveillance and follow-up, vigilance- Advertising control and packaging validation.
- Strategiqual ConsultingMarket Access Director - Senior ConsultantCONSULTING AND AUDITSJanuary 2021 - January 2024 (3 years)Paris, France- Consulting with senior expertise for companies in the medical device sector in Market Access, Regulatory Affairs, and Quality Management- Carrying out missions related to medical devices in collaboration with manager and operational consultants- Drafting regulatory analyses or operational mission deliverables;- Management of the Medical Device Market Access department- Project and human resource management- Participation in the company's promotional activities and representation in institutional activities.- Participation in the development of new services and strategic thinking on company organization
- Cabinet White-TilletTeam Manager - Senior ConsultantCONSULTING AND AUDITSJanuary 2014 - January 2021 (7 years)Paris, FranceStrategy, consulting, regulatory and quality support from design to post-market.- EU Regulation 2017/745 on medical devices- Technical documentation, CE marking, compliance procedures- Clinical Evaluation Report (CER)- Risk Management File (ISO 14971)- Post-market clinical follow-up, vigilance.- Implementation of quality systems, support, audits (ISO 13485)- Reimbursement (generic online registration, individual identification code, drafting of brand-name registration files).- Advertising control and packaging validation.- Trainer for companies on regulation and quality.- Participation in the development of programs/schedules and in the animation of inter-company training.- Preparation of quotes, response to tenders, and client management.- Recruitment, supervision, and training of collaborators.- Management of consultants, experts, and partner companies.
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Education
- State Diploma of Doctor of PharmacyFACULTY OF PHARMACY PARIS2015Diplôme d'état de Docteur en Pharmacie
- Master 2 Regulatory Affairs for Health ProductsFACULTY OF PHARMACY CHATENAY-MALABRY2014Master 2 Affaires Réglementaire des produits de santé