Alongside validation, risk-based qualification is a central element of quality assurance in GxP-regulated industries, such as the pharmaceutical industry or medical technology. From the qualification of individual devices to the qualification and validation of complex plants, GMP upgrades or new construction projects in the compliance area, Testo Industrial Services offers you the necessary manpower, the know-how and the appropriate measurement technology individually and according to your needs.
Qualification - ensuring high quality in a GMP-compliant manner
Our service for you
- Support from individual measurements to project management
- Qualification support across all qualification phases - DQ, IQ, OQ and PQ
- Establishment of risk management and implementation of risk analyses
- Preparation of the qualification documents and reports
- Carrying out all qualification tests and measurements
- Complete coordination of your project
- We share our practice-oriented expert knowledge and know-howwith you
- Design and consulting quality assurance for risk-based planning and qualification of cleanrooms, plants and utilities, equipment as well as transport systems and storage areas
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Cleanroom qualification
Safety and compliance for your cleanrooms
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Qualification of plants & utilities
Ensures process stability and robustness
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Transport and storage qualification
GxP services for storage areas, packaging and transport systems
Your advantage: Our competence
- Expertise: Consulting quality assurance, measurements, project management - our industry-experienced team supports you precisely & in line with your needs
- Technology: The use of our measuring equipment with more than 4,500 references ensures reliable measurement and test results.
- Documentation: We hand over the documentation in the audit-proven layout or individually according to customer requirements to you personally on completion of the order.
Risk management
In order to ensure the overall goal of patient safety, potential defects and hazards to product quality must be identified and brought under control. For this purpose, it is advisable to establish a comprehensive process of risk assessment, control and monitoring throughout the product life cycle.
We have been intensively involved in risk analysis and risk management for many years and know your requirements exactly. Our industry-experienced GxP Services team supports you in identifying weak points and risks with regard to product quality and patient safety, as well as in defining control measures and implementing them in the course of qualification and validation. Together we optimise your quality risk management.
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This is how we support you in your quality risk management:
- Structuring and planning of compliance activities for sound risk management according to ICH Q9/EU-GMP Part III
- Integration of all project participants in the risk management process
- Structuring, preparation and moderation of risk analyses according to established methods (e.g. FMEA)
- Advice & support for the implementation of a risk management strategy
GxP Services Team
Professional competence, experience and high-precision equipment. The engineers and technicians of our GxP-Services Team are on duty for you throughout Europe.
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GxP services made to measure
More service, more security for your GxP compliance. Full service and know-how for your requirements.
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Success stories
We support you in your projects and are committed to your goals. Here you will find an excerpt from the references of our successful GMP projects.
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Losan Pharma GmbH
Full-service support: cleanroom qualification and calibration
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Paul Hartmann AG
New clean room construction: Project support & qualification
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Grünenthal GmbH
Solids production: Qualification of a tablet line
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Know-how
In our Knowledge Centre you will find answers from our experts to numerous questions about qualification.