Safety report - Import export

The CPSR consists of two parts, A and B: in Annex I of the Cosmetics Regulation, all the information that must be collected and processed by the Safety Evaluator in order to identify and quantify the dangers that the cosmetic product may present for the human health, namely: PART A contains information on the safety of the cosmetic product, such as: 1. Quantitative and qualitative composition of cosmetic products; 2. Physical/chemical characteristics and stability of the cosmetic product; 3. Microbiological quality; 4. Impurities, traces, information on packaging material; 5. Normal and reasonably foreseeable use; 6. Exposure to the cosmetic product; 7. Exposure to substances and calculation of the MoS; 8. Toxicological profile of substances; 9. Undesirable effects and serious undesirable effects; 10. Information about the cosmetic product. PART B holds the conclusion, the warnings and instructions of use to label, the scientific reasoning and the assessor's diploma.

Manufacturing cosmetic products comes with a great deal of quality decisions and responsibilities in terms of raw materials’ selection, formula compliance, clients’ expectations, markets requirements, data collection,... What if you had a regulatory partner who is willing to relieve you from some of this burden to make your life and the life of the cosmetic brands contacting you much easier? With our manufacturer program, we have got you covered! We can: - Introduce you to cosmetic raw material suppliers that match your specifications. - Introduce you to our international clients and promote your services to them. - Prepare the cosmetic product safety report part A. When you choose Taobé as your regulatory partner and have your cosmetic formula pre-checked for compliance, we automatically tell you when an upcoming regulatory change impacts one of your cosmetic ingredients. Taobé has also developed an online tool to collect and keep safe your confidential data.

Proximity Warning, powered by Lopos, is an optional add-on crafted to elevate workplace safety in warehouses and while using forklifts. This 360° proximity warning system delivers crucial alerts and actionable insights to mitigate incidents and cultivate a secure work environment. By minimising impacts between forklifts, the system aids in averting damage and downtime, safeguarding both your equipment and employees. Additionally, it serves as a vital measure to reduce collisions between forklifts and pedestrians, ensuring a workplace that prioritises safety. Proximity Warning delivers detailed reports on near-misses. This information enables the identification of operators and pedestrians prone to accidents, facilitating proactive measures to enhance overall safety.

We offer you the following services: - Regulatory Advice - REACH Registration - Preparation of Registration Dossiers - Read Across - IUCLID - Robust Study Summaries - Chemical Safety Report / CSR - Toxicological Expertise - Optimal Test Strategy Development - REACH Testing: Tests and Studies acc. GLP - REACH Study Monitoring - SVHC Screening - Risk Assessment - REACh Compliance Service / REACh Auditing Service - REACH Material Safety Data Sheets We would also be happy to be your REACH service provider, who reliably looks after your REACH projects, just as we already do for many other satisfied customers. For more information please contact INVITRO-CONNECT GmbH. Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com REACH Service - All REACH laboratory tests - Phys-Chem / Tox / in vitro tests / Genotox / Ecotox, etc. - More than 80 test laboratories - Study monitoring, Regulatory Service, IUCLID 6, CSR etc.

Our experts support you with the following services: - Toxicological assessment within the framework of the REACH and biocide regulations - Environmental Risk Assessment (ERA = Environmental Impact Assessment), e.g. for pharmaceuticals - Literature research and evaluation - Examination of the reliability and validity of the studies carried out (according to OECD guidelines, EU methods or according to Klimisch et al. 1997) - Assessment of relevant toxicological endpoints, e.g. acute toxicity, genotoxicity, irritation / corrosion of the skin or eyes - Evaluation of all relevant toxicological, ecotoxicological endpoints, e.g. freshwater organisms (daphnia, algae, fish) - Read Across - Study monitoring of studies - Creation of the Endpoint Summaries and Endpoint Study Records for IUCLID (REACH and biocidal active ingredients and products) - Safety assessment and safety report for cosmetic products - Water hazard class - etc. Questions?--> contact@invitro-connect.com