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I am heading a fast-growing regulatory affairs firm in India that is now taking on European cosmetic compliance work. Our immediate requirement is for a European-registered toxicologist (ERT) who can review and formally sign off more than 25 Cosmetic Product Safety Reports (CPSRs). Here is what the engagement involves: • Carefully examine each CPSR to be certain it meets all current EU cosmetic safety regulations. • Flag any data gaps or formulation concerns and advise on revisions so the file is fully compliant. • Once each report is satisfactory, add your electronic signature, credentials, and ERT registration details. • Return a brief sign-off statement or certificate for our own records. Acceptance criteria A CPSR is considered complete once the signed toxicologist declaration is included, referencing the specific product name and date, and the final PDF is delivered back to us. Ideal background Because these are cosmetics, I need someone who already works in this sector, holds ERT certification, and is an active member of the relevant professional regulatory body. Previous collaboration with Indian brands is a plus, but not essential. All files are ready in English, supported by raw toxicological profiles, stability data, and GMP statements. I can share a sample report under NDA so you can gauge the work level before we start. If you are available to take on the first batch right away and can commit to timely turnaround, I would like to hear how you normally structure milestones for multi-report projects and confirm your membership details.
Project ID: 40511797
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5 freelancers are bidding on average $990 USD for this job

As a senior toxicologist with extensive experience in cosmetic safety assessments, I understand the critical importance of ensuring compliance with EU regulations for your fast-growing regulatory affairs firm. Your need for a European-registered toxicologist to meticulously review and sign off on over 25 Cosmetic Product Safety Reports (CPSRs) aligns perfectly with my background in this sector. Having worked directly within EU frameworks, I am adept at identifying data gaps and formulation concerns that may compromise compliance. My familiarity with documentation processes ensures that each CPSR not only meets stringent standards but also includes the requisite ERT certification details. I typically structure milestones based on the complexity of reports, allowing for thorough reviews and timely feedback. I can start reviewing your first batch promptly, maintaining an efficient turnaround. Could you share specific timelines you have in mind for completing these reports? This will help me align my workflow to meet your expectations effectively.
$1,500 USD in 7 days
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Hello, I am interested in supporting your cosmetic compliance documentation project. While I am not an ERT signatory, I can assist with the preparation and review process to help ensure CPSR files are complete, well-organized, and ready for toxicologist assessment. My support can include: • Reviewing reports for completeness and consistency • Organizing toxicological profiles, stability data, and GMP documentation • Identifying missing information and documentation gaps • Formatting and preparing CPSR files for final regulatory review • Maintaining accurate records and project tracking across multiple reports I am detail-oriented, comfortable working with technical documentation, and committed to meeting deadlines. I can begin immediately and provide regular progress updates throughout the project. If you are open to support assistance alongside the final toxicologist sign-off process, I would be happy to review a sample report under NDA and discuss the workload further. Thank you for your consideration. Best regards, [NUR ALIESYAH DALILAH]
$750 USD in 6 days
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Hi, Thank you for the detailed brief. I have reviewed the project and I am interested in discussing how I can support your firm with this engagement. I understand you need a European-registered toxicologist to review and sign off more than 25 CPSRs in line with current EU cosmetic safety regulations. I can carefully examine each report, identify any data gaps or formulation concerns, advise on necessary revisions, and provide the formal toxicologist declaration with credentials and ERT registration details for each completed file. For multi-report projects like this, I typically structure milestones in batches. I suggest starting with a first batch of 5 reports so we can align on expectations, turnaround time, and any formatting preferences before proceeding with the remaining files. This keeps the workflow clean and allows for quick adjustments if needed. I am happy to sign an NDA and review a sample report before we begin to confirm the work level and provide a realistic timeline commitment. Please feel free to share more details so we can confirm the scope and get started on the first batch right away. Best regards, (Nurfaraizah binti indera safri)
$1,050 USD in 20 days
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