Installation
Certified installation for compliance with regulatory and internal requirements
Your individual requirements are the basis for our various service packages for certified Installation.
We take the on-site measurement conditions into consideration to ensure that your measurement devices deliver precise, highly accurate and reproducible measurement results.
Installation by our trained specialists includes a user-specific installation with detailed instructions on all device functions. This ensures the fulfilment of compliance with regulatory requirements, including internal and external guidelines.
We certify the entire installation and device training by means of a commissioning protocol or with certified documents from the DQ-IQ-OQ-PQ qualification.
Each working environment demands different specifications for the installation of the measurement devices. The three Krüss service packages for installation meet different requirements:
Installation
Our service experts will be happy to carry out the installation of your new KRÜSS measurement instruments on your premises.
After successful installation and functional testing, your employees will receive instruction and user training. We are happy to answer any questions you may have during installation and provide helpful expert tips. For example, you will receive professional tips for cleaning or calibrating your new measurement instrument. The entire installation is documented for you with a training log.
This installation package is suitable for all customers who work in compliance with GMP or ISO9000.
Our services as a survey:
- Installing and setting up the device functions
- Installation and simple function test on site
- Instruction and user training
- Documentation of the installation with a personalized training log
Installation including IQ/OQ/PQ qualification
This installation is extended by a documented qualification of the new measurement instruments and extensive on-site inspections.
The IQ/OQ/PQ service ensures that the necessary quality requirements for the measurement instrument and thus regulatory requirements are reliably met. The entire service is documented in a commissioning report and includes the following qualifications:
- Installation qualification (IQ): Documented proof that your new device has been installed in accordance with GMP-critical requirements. Measurement and control technology, installed components, surfaces and add-on parts are tested.
- Performance qualification (OQ): Documented proof that the system specifications are fully achieved over the entire measurement range.
- Performance qualification (PQ): Documented proof that all relevant system components and other relevant systems, comply with defined specifications and requirements during operation.
With this installation package, we support customers who are subject to regulatory requirements when installing their new measurement instruments, including, for example, specification criteria of the European Union or the US Food and Drug Administration (FDA).
Services at a glance
- Qualification sample documents for internal approval
- Comprehensive device qualification with detailed procedure description (flow chart)
- Method pre-configuration for required measurement applications
- Setting up routine checks and checks for the user applications
- On-site calibration with traceable norms and standards covering all important calibration parameters
- Comprehensive training and instruction for users and device managers
Installation in the pharmaceutical industry
The GMP-compliant manufacture of medicinal products and active ingredients is a prerequisite for successful marketing authorization. Quality assurance plays a very central role here, as deviations in quality can have a direct impact on consumer health.
In order to comply with the strict guidelines of the European Union or the US Food and Drug Administration(FDA), the measurement devices that measure must be qualified. The qualification is divided into four phases:
- Design qualification (DQ)
- Installation qualification (IQ)
- Performance qualification (OQ)
- Performance qualification (PQ)
Our experts have developed a qualified range of services for installation in the highly regulated pharmaceutical sector. With our premium installation, we ensure that the necessary quality requirements for the measurement instruments and thus the official specifications are reliably met and documented. As a direct result, the necessary process validation has been completed successfully in the lab.
Installation (on-site service) for highly regulated laboratory analysis complies with the following guidelines:
- GAMP5
- GMP
- USP1058
- and 21 CFR Part 11
Our services as a survey:
- DQ support by processing customer specifications
- Includes all necessary IQ/OQ/PQ services in the working environment of our customers
- Preparation of all necessary test reports, documents and certificates with traceable documents
- Including the provision of all certified test equipment required for qualification as well as measuring, inspection and special tools
- Also includes SOP(Standard Operating Procedures) support based on security aspects of audit trail, user management and data integrity
- Including extensive application-related training for users
Supplementary information on DQ/IQ/OQ/PQ
Device qualification ensures laboratory operation according to reproducible procedures
All A.KRÜSS qualification solutions comply with the “risk-based” approach introduced at millennium. The devices are checked and installed by our experts using traceable test equipment. With a 4-step device qualification, you receive proof of quality and process reliability.
- The DQ is the documented proof that the planned design of the device is suitable for the intended use.
- The IQ confirms the complete, specified delivery and correct installation. Devices and their parts are identified, device configurations are verified and manufacturer specifications for trouble-free operation are documented.
- The OQ proves whether the device is working according to plan and regulations. Users receive, among other aspects, useful information for the SOP (Standard Operating Procedure) and user training.
- The final PQ is the performance check of the devices according to a defined procedure. It provides proof that the DQ process requirements are fulfilled under real conditions. The aim is to release the devices for laboratory use and ensure that they meet the requirements of regulatory authorities, standards, guidelines, audits and internal quality assurance.
Our qualification is designed to save you costs, resources and time in the process. Our specialists have many years of experience in the qualification of measurement instruments and are familiar with the current regulatory requirements of the applicable directives, standards and laws. Below is a selection of the specifications that are important to us:
- EC GMP Guide
- cGMP rules for medical devices
- Good Automated Manufacturing Practice (GAMP) guidelines
- FDA-compliant qualification of systems (21CFR Part11)
- Pharmacopoeia or USP pharmacopoeia requirements
- DAkkS guidelines
- In accordance with the requirements of DIN EN ISO 17025
Our qualifications are carried out with a reduction of effort to a justifiable level, without piles of paper and with comprehensible documents.
Your advantages at a glance:
- You may request the documents for viewing in advance.
- We work with the necessary special tools and measuring equipment (traceable standards) and have a great deal of expertise in test equipment management, risk assessment and risk analysis.
- Digital devices are subject to strict data integrity checks. That’s why we initialize the correct and suitable device firmware configuration for you.
- We work with electronic signatures, by meaning the uniqueness of the combination of user ID and password.
- The data documentation is flanked by a two-stage audit trail and audit trail log concept.
- You will receive extensive training. This guarantees that all software applications integrate perfectly into your work processes.