QbD Group
    申请审计联系我们
    按行业浏览服务
    Extractables & Leachables Reports – Expert toxicological assessments for packaging and device safety

    Extractables & Leachables Reports

    Expert toxicological assessments for packaging and device safety

    QbD Group provides toxicological assessments and risk evaluations for extractable and leachable impurities, designed to fit your specific needs and ensure compliance with FDA, EMA, and ICH standards.

    What are extractables & leachables reports?

    The risk and toxicological assessment of extractable and leachable impurities is a crucial process in the pharmaceutical industry to ensure the safety and quality of products.

    These impurities, which can migrate from packaging materials or medical devices into the final product, represent a potential risk to patients. Regulators such as the FDA and EMA require detailed reports to support the safety of drugs and medical devices.

    Extractables & Leachables Reports — QbD Group

    How can we help?

    Our team of toxicologists and analytical chemists work together to perform in-depth analyses, risk assessments, and toxicological evaluations.

    Risk assessment

    Analysis of possible compounds released from drug contact materials, assessing their impact on safety and determining safe limits.

    Toxicological evaluation

    For all impurities outside established limits — compilation of harmful effects, toxicity determination, and health risk assessment using QSAR methods.

    Customized reports

    Reports tailored to meet specific regulatory requirements for each pharmaceutical product and client.

    Regulatory alignment

    Compliance with FDA, EMA, USP 1663, USP 1664, and ICH Q3E guidelines.

    Our process

    We provide customized reports that meet the specific regulatory requirements for each pharmaceutical product and client.

    1. Initial consultation

    Understand your specific materials and regulatory context.

    2. Material analysis

    Identify potential extractable and leachable compounds from packaging and device materials.

    3. Risk & toxicological assessment

    Evaluate safety impact and determine whether impurities are within safe limits.

    4. Report preparation

    Deliver comprehensive, submission-ready reports aligned with regulatory standards.

    Extractables & Leachables Process — QbD Group
    QbD Group expertise

    为什么选择QbD Group

    您值得信赖的合作伙伴

    We combine in-depth technical knowledge with a detailed understanding of international regulations, ensuring customized and rigorous reports.

    Specialized, multidisciplinary team of toxicologists and analytical chemists.

    Customized reports according to the specific regulatory requirements and needs of each client.

    Approach combining in-depth technical knowledge with understanding of international regulations.

    AETOX membership and EUROTOX certification

    the highest professional standards.

    FAQ

    Frequently Asked Questions

    聊聊毒理学

    无论您需要 PDE 报告、亚硝胺风险评估还是 REACH 支持,我们的认证毒理学家都已准备好为您提供帮助。

    我们使用 Cookie 来改善您的体验

    我们使用必要的 Cookie 来保证网站功能,以及可选的分析 Cookie 来改善我们的服务。 阅读我们的 隐私政策Cookie 政策.