One-Stop-Shop solution to meet all your global regulatory challenges.

Eurofins Regulatory and Consultancy Services supports pharmaceutical drugs company to select the right path to guarantee safety and quality. Our team helps to deal with regulatory challenge leveraging on a science- and risk-based approach. Our experience in diverse manufacturing and regulatory settings (from small molecule to biologics and ATMPs) ensure our clients needs are fully understood and easily transformed in solid strategies.

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Our Services

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E&L and Qualification

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Toxicological & chemical safety assessment

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Nitrosamines risk & control strategy

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Validation & qualification consulting

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Biologics & ATMP regulatory strategy

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Environmental compliance

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Scientific strategy & risk-based optimisation

Child holding a medical device, highlighting the importance of usability and risk analysis in ensuring device safety for vulnerable users.

Customised consulting

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Biocides regulatory strategy and authorisation

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Biocides scientific & strategic consulting

    

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Chemicals & Disinfectants Regulatory Compliance

Latest regulatory updates

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Clinical Phases – Documentation & Validation

Registration – Regulatory Submission Support

Commercialisation – Change & Gap Assessment

Post-Market – Lifecycle Documentation & Compliance

Our trainings

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Meet our experts

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Book your free 30-minute session with our experts

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Latest regulatory update

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