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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.

Regular audits

Employee training

Adaptability

Adaptability

Why are 3rd party audits in pharma and biotech?

  • Fulfilment of regulatory requirements (GMP regulations and guidelines)

  • Qualification of suppliers and service providers beyond mere certificates

  • Sicherstellung der Compliance in der gesamten Lieferkette

  • Risikominimierung durch unabhängige Experten-Audits

  • 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.

Q-Schraege

CONTACT

We look forward to receiving your enquiry.

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