- Pharmaceutical & Biotech Industry
- Medical Devices
- Cosmetics
- Veterinary Medicinal Products
- Agrochemicals & Food Additives
- GLP: Good Laboratory Practices
We support our client on the safety assessment of cosmetic products in accordance with the requirements of the cosmetic directive and regulation in force.
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The safety assessment will be based on available peer-reviewed toxicology literature, MSDSs, trade association documents, and governmental listings and databases. In the case that available information from these sources is insufficient, and if experimental evidence is required, we would monitor CROs capable of carrying out in vitro toxicology studies in accordance with appropriate guidelines.
We give support on evaluating relevant toxicological information on each ingredient to complete the product information file.
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We also carry out the safety assessment of each ingredient and the final cosmetic product, and issue the cosmetic product safety certificate.
We offer our customers the design of toxicological programs for each new cosmetic ingredient.
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We also assist on the toxicological study design, selection of suitable CROs around the world (considering expertise, slots and prices), requests for cost estimates to CROs, definition and critical review of protocol to ensure regulatory compliance, management tasks, direct communication with study directors, follow-up / monitoring of all study activities, coordination of tasks in multisite studies, assistance on any decisions along the study, interpretation of study results and critical review of the study report.
We also perform a safety assessment of new ingredients based on toxicology study results.
