Impurities
Are you looking for certificated toxicology reports to support your production process & compliance with regulations?
Do you need risk assessment or toxicological evaluations of impurities in pharmaceutical products?
QbD offers the largest online library of high-quality available toxicology reports certificated by AETOX members.
Why it is necesary?
EUROTOX toxicologist signs our Toxicology Impurities reports and are essential for evaluating risks and impurities in the manufacturing of drugs, vaccines, biologicals, ATMP, Medical Devices, and IVD. These assessments, covering various impurities, are crucial for QA personnel, Compliance Officers, Site Directors, and Technical Directors.
The significance lies in supporting safety procedures, ensuring compliance with regulations, and safeguarding both the products and workers in the manufacturing process. The necessity arises from the need for a well-documented repository of updated certified reports, vital for audits and inspections, ultimately contributing to the overall safety of pharmaceutical production.
We can help you with Risk assessment reports and Toxicological evaluations of impurities (nitrosamines, organic impurities, mutagenic impurities, elemental impurities and impurities from extractables and leachables studies).
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Why QbD Group?
More than 10 years providing Toxicology Services, QbD is your partner for advice and support on controlling quality risks.
QBD Toxicology team is a member of AETOX organization and the experts are certificated by EUROTOX.
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Tailored solutions
The actual approach of this service is up to you. It is fully tailored to your needs.
Contact us
Don’t hesitate to contact us so we can listen to your needs and provide you with the right service.
