Freelancer profile translated to English.
Back to original languageAbout Camille
After 12 years in an R&D department in the cosmetic industry as a regulatory affairs manager, I wanted to support and advise brands in bringing their cosmetic products to market in Europe and abroad by creating INSIDE COSMETICS.
My expertise in cosmetic regulations will allow you to refocus and dedicate yourself fully to the development of your cosmetic products.
My goal is to support you effectively to ensure the success of your brand.
✅ Product Information File (PIF)
✅ Formula validation
✅ Labeling and communication material validation
✅ Advice on test selection based on claims
✅ Test management and planning
✅ CPNP notification
✅ Obtaining labels
✅ Regulatory watch
...
Do not hesitate to contact me for your projects, I would be delighted to help you!
French
Native or bilingual
Can work on-site
Aix-en-Provence (up to 50km)
Experience
- Inside CosmeticsFreelance in Cosmetic Regulatory AffairsFASHION AND COSMETICSJuly 2022 - Today (3 years and 11 months)Provence-Alpes-Côte d'Azur, France💼 Cosmetic Regulatory Affairs ConsultantAre you developing a cosmetic product and want to bring it to market in full compliance?I assist brands and contract manufacturers at every regulatory stage to secure the marketing of their products.🔎 My expertise:- Creation and updating of the Product Information File (PIF)- Compliance check: formula, labeling, claims- CPNP notification- Regulatory review of communication materials- Regulatory watchFor 4 years, I have been supporting young brands, established brands, and contract manufacturers in managing and securing their cosmetic projects.🎯 My goal: to offer you tailor-made support to launch your products with peace of mind in France, Europe, and internationally.
- Thalgo CosmeticCosmetic Regulatory Affairs ManagerFASHION AND COSMETICSDecember 2010 - May 2022 (11 years and 6 months)Roquebrune-sur-Argens, France>> ELLA BACHE and THALGO Brands- Analysis of the regulatory compliance of raw materials- Management of safety tests- Compilation of data for safety assessment by the toxicologist- Drafting of Product Information Files (PIF)- Notification on the European CPNP portal- Support in choosing efficacy tests based on chosen claims- Review and validation of labeling- Review and validation of communication tools (posters, brochures, website…)- Drafting of claims files- Drafting of documents required for international product registration+ Management of outsourced projects - reference regulatory contact+ Regulatory watch: analysis and study of the impact of new regulations, communication to relevant departments, proposal of action plan and monitoring of its implementation
- EurofinsCosmetic Clinical Study ManagerPHARMACEUTICALS INDUSTRYSeptember 2009 - September 2010 (1 year)Aix-en-Provence, France- Implementation of cosmetic clinical studies (development of laboratory notebooks and study documents),- Performance of instrumental measurements- Verification of study data and documents- Analysis of results- Drafting of clinical study reports (French, English)- Updating of operating procedures and commercial brochures for efficacy tests- Research & Development of cosmetic clinical study protocols
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Education
- Master of ManagementUniversity of Montpellier2010Master 2 (M2), Management de projet / Produit de santé
- Master 1, R&D Product for Health and CosmeticsUniversity of Montpellier2009Master 1, R&D Produit de Santé et Cosmétiques
Skill set
Categories
- Other