Regulation and Safety of Cosmetics: Pre- and Post-Market Considerations for Adverse Events and Environmental Impacts

Cosmetic products have been increasingly regulated, particularly in Europe. With the introduction of the cosmetic regulation in 2013, stricter quality standards were implemented, surpassing those set by the 1976 legislation. The primary objective of these regulations is to safeguard consumer safety...

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Main Authors: Daniela Vieira, Joana Duarte, Pedro Vieira, Maria Beatriz S. Gonçalves, Ana Figueiras, Alka Lohani, Francisco Veiga, Filipa Mascarenhas-Melo
Format: Article
Language:English
Published: MDPI AG 2024-10-01
Series:Cosmetics
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Online Access:https://www.mdpi.com/2079-9284/11/6/184
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author Daniela Vieira
Joana Duarte
Pedro Vieira
Maria Beatriz S. Gonçalves
Ana Figueiras
Alka Lohani
Francisco Veiga
Filipa Mascarenhas-Melo
author_facet Daniela Vieira
Joana Duarte
Pedro Vieira
Maria Beatriz S. Gonçalves
Ana Figueiras
Alka Lohani
Francisco Veiga
Filipa Mascarenhas-Melo
author_sort Daniela Vieira
collection DOAJ
description Cosmetic products have been increasingly regulated, particularly in Europe. With the introduction of the cosmetic regulation in 2013, stricter quality standards were implemented, surpassing those set by the 1976 legislation. The primary objective of these regulations is to safeguard consumer safety during the use of cosmetic products. Despite these advancements, certain regulatory gaps remain, indicating the need for more effective measures to enhance human and environmental health protection. Considering the aforementioned, this work aims to provide an overview of the current Cosmetics Regulation, highlighting the weakest cornerstones that represent the missing link keeping the core objective from being achieved. While there is ongoing reliance on historical data from animal studies, efforts are actively underway to replace these methods with new new approach methodologies for risk assessment. Additionally, regulatory authorities continue to improve environmental considerations in the assessment process. These measures, along with enhanced surveillance systems, are gradually addressing existing gaps and contributing to a more robust regulatory framework that balances market access with consumer safety. Legally non-compliant—or perhaps compliant but unknowingly dangerous—products may be used by people who relativize them as inherently safe, leading to adverse events. Whether caused by an underlying disease or purely by the chemical’s toxicity, these may never come to the attention of the authorities as they are generally under-reported, making it unfeasible to implement corrective or preventive measures to address their root cause. To illustrate, non-compliant products that have been detected by the Portuguese authority, INFARMED, I. P., from January 2018 to September 2023 are discussed, which were found to be potentially dangerous to human health and, therefore, withdrawn from the market.
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spelling doaj-art-3cfe7ccd36764bdea8ff7ef823f017182024-12-27T14:19:18ZengMDPI AGCosmetics2079-92842024-10-0111618410.3390/cosmetics11060184Regulation and Safety of Cosmetics: Pre- and Post-Market Considerations for Adverse Events and Environmental ImpactsDaniela Vieira0Joana Duarte1Pedro Vieira2Maria Beatriz S. Gonçalves3Ana Figueiras4Alka Lohani5Francisco Veiga6Filipa Mascarenhas-Melo7Drug Development and Technology Laboratory, Faculty of Pharmacy of the University of Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, PortugalAbel Salazar Institute of Biomedical Sciences (ICBAS), University of Porto, Rua Jorge Viterbo Ferreira 228, 4050-513 Porto, PortugalInstitute of Pharmacology & Experimental Therapeutics, Coimbra Institute of Clinical and Biomedical Research (iCBR), Faculty of Medicine and Center for Innovative Biomedicine and Biotechnology (CIBB), University of Coimbra, 3000-548 Coimbra, PortugalDrug Development and Technology Laboratory, Faculty of Pharmacy of the University of Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, PortugalDrug Development and Technology Laboratory, Faculty of Pharmacy of the University of Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, PortugalAmity Institute of Pharmacy, Amity University, Noida 201313, Uttar Pradesh, IndiaDrug Development and Technology Laboratory, Faculty of Pharmacy of the University of Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, PortugalLAQV/REQUIMTE, Group of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, PortugalCosmetic products have been increasingly regulated, particularly in Europe. With the introduction of the cosmetic regulation in 2013, stricter quality standards were implemented, surpassing those set by the 1976 legislation. The primary objective of these regulations is to safeguard consumer safety during the use of cosmetic products. Despite these advancements, certain regulatory gaps remain, indicating the need for more effective measures to enhance human and environmental health protection. Considering the aforementioned, this work aims to provide an overview of the current Cosmetics Regulation, highlighting the weakest cornerstones that represent the missing link keeping the core objective from being achieved. While there is ongoing reliance on historical data from animal studies, efforts are actively underway to replace these methods with new new approach methodologies for risk assessment. Additionally, regulatory authorities continue to improve environmental considerations in the assessment process. These measures, along with enhanced surveillance systems, are gradually addressing existing gaps and contributing to a more robust regulatory framework that balances market access with consumer safety. Legally non-compliant—or perhaps compliant but unknowingly dangerous—products may be used by people who relativize them as inherently safe, leading to adverse events. Whether caused by an underlying disease or purely by the chemical’s toxicity, these may never come to the attention of the authorities as they are generally under-reported, making it unfeasible to implement corrective or preventive measures to address their root cause. To illustrate, non-compliant products that have been detected by the Portuguese authority, INFARMED, I. P., from January 2018 to September 2023 are discussed, which were found to be potentially dangerous to human health and, therefore, withdrawn from the market.https://www.mdpi.com/2079-9284/11/6/184cosmetic regulationsafety assessmentcosmetovigilancequality defectsregulatory affairsanimal testing
spellingShingle Daniela Vieira
Joana Duarte
Pedro Vieira
Maria Beatriz S. Gonçalves
Ana Figueiras
Alka Lohani
Francisco Veiga
Filipa Mascarenhas-Melo
Regulation and Safety of Cosmetics: Pre- and Post-Market Considerations for Adverse Events and Environmental Impacts
Cosmetics
cosmetic regulation
safety assessment
cosmetovigilance
quality defects
regulatory affairs
animal testing
title Regulation and Safety of Cosmetics: Pre- and Post-Market Considerations for Adverse Events and Environmental Impacts
title_full Regulation and Safety of Cosmetics: Pre- and Post-Market Considerations for Adverse Events and Environmental Impacts
title_fullStr Regulation and Safety of Cosmetics: Pre- and Post-Market Considerations for Adverse Events and Environmental Impacts
title_full_unstemmed Regulation and Safety of Cosmetics: Pre- and Post-Market Considerations for Adverse Events and Environmental Impacts
title_short Regulation and Safety of Cosmetics: Pre- and Post-Market Considerations for Adverse Events and Environmental Impacts
title_sort regulation and safety of cosmetics pre and post market considerations for adverse events and environmental impacts
topic cosmetic regulation
safety assessment
cosmetovigilance
quality defects
regulatory affairs
animal testing
url https://www.mdpi.com/2079-9284/11/6/184
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