3rd party audits for pharma and biotech
We check the quality of your components.
Our services in the area of 3rd party audits
In the highly regulated pharmaceutical and biotech industry, ensuring quality and compliance along the entire supply chain is crucial. Our engineering office offers you professional 3rd party audits to qualify and monitor your suppliers and service providers according to the strict GMP requirements.
Why are 3rd party audits in pharma and biotech?
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Fulfilment of regulatory requirements (GMP regulations and guidelines)
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Qualification of suppliers and service providers beyond mere certificates
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Sicherstellung der Compliance in der gesamten Lieferkette
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Risikominimierung durch unabhängige Experten-Audits
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Entlastung Ihrer internen Ressourcen
Our approach: Expertise, transparency and efficiency
Preparation: Careful analysis of your specific requirements and the company to be audited
Implementation: On-site audit by experienced experts with in-depth technical and regulatory knowledge.
Documentation: Preparation of detailed and meaningful audit reports
Action planning: development and testing of CAPA measures
Follow-up: Ensuring implementation through follow-up audits
Your added value through our 3rd party audits
01
Compliance Security
Fulfilment of all relevant GMP requirements in the supply chain.
02
Risk minimisation
Frühzeitige Erkennung und Behebung von Schwachstellen.
03
Resource optimisation
Relief for your internal quality department.
04
Global coverage
Global auditing with local expertise.
05
Continuous improvement
Sustainable increase in supplier quality.