Annalisa Lovera
Regulatory Affairs Specialist @Chemsafe Srl
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WORK HISTORY
Regulatory Affairs Specialist @Chemsafe Srl
Piedmont, IT
Comprehensive consultancy related to European Regulations: BPR, REACH/SDS authoring (according to 878/2020 and HCS 2012) and CLP/GHS criteria application for substances/mixtures C&L. PCN according to Annex (and previous notification to Poison Centre according to National legislation in various European Countries)- Management of transitional period (BPR, Art.89) Product authorizations in various European countries (i.e. Portugal, The Netherlands, Spain, Greece, Belgium) and Italy (PMC)- Regulatory framework evaluation for borderline products (biocides, detergents, cosmetics, medical devices, free sale)- Interaction with European Competent Authorities pre- and post- Biocidal Product Authorization- Communication with laboratories for efficacy/chemical-physical and hazard properties studies- Evaluation of Active Substance Annex I BPR inclusion- Human Health and Environmental Risk Assessment for Biocidal Products for different PT (PT 1-5; PT8, PT18 and PT21).
EDUCATION
Università degli Studi di Torino
II° Level Master in Pharmaceutical Technologies and Regulatory Affairs, Medicinal and Pharmaceutical Chemistry
Università degli Studi di Torino
Master of Science - MS, Medicinal and Pharmaceutical Chemistry
ABOUT ANNALISA LOVERA
Pharmaceutical chemist with a deep experience in Chemicals compliance to EU and national…
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