Medical Device Compliance
The QMS system described by ISO 13485 is tailored to medical devices, similar to the requirements of ISO 9001 but significantly more extensive in terms of overall effort and implementation.
Special features serve the quality requirements of medical devices. They must be observed when setting up a quality management system in accordance with ISO 13485 and mapped in the quality management manual. This includes the design documents and the development file for the respective medical device as well as the verification and validation of the described design.
Regardless of whether it is a question of checking the ISO compliance of an existing system or planning, setting up and implementing a new QM system, our experts will advise, support and assist you actively and competently!
Depending on your needs, we offer consulting, processing of individual subtasks or complete implementation of the ISO 13485 system.
On the basis of Gap analysis (audits), we determine compliance with the standard and support you in implementing the resulting measures.
The update and implementation of QM systems in relation to the requirements of the revision ISO 13485:2016 is implemented through conceptual work and the creation of documents. In doing so, we apply risk-based considerations to all business processes.
The preparation of the design documents and the development file according to ISO 13485 section 7.3 and/or FDA Design Control 21 CFR 820.30 is also part of our service portfolio.
Due to our long experience in the field of verification and validation of manufacturing processes for medical devices, we create the appropriate validation concept for your product based on the current standards and regulations.
This also includes the qualification of equipment and facilities. Here we know exactly what is important and what is necessary and indispensable. Our motto is "As little as possible but as much as necessary" and guarantees you an efficient approach.
We support you in the practical implementation of the concept, with the aim of providing objective proof that your product meets all regulatory and customer requirements.
If personnel resources are required, we can also take over the function of the quality management representative temporarily.
Additional medical device qualification services can be found here: Qualification for Medical Device Industry.
A systematically applied quality risk management ensures the consistent performance of processes and the high quality of products.
Valicare GmbH supports companies of the medical device industry in the fulfillment of the central requirements of the national and international regulations such as EN ISO 13485, 21 CFR Part 820 with cGMP, GHTF documents or GAMP 5 using the risk-based approach.
The quality risk management is applied in the general consideration of the criticality of the processes in the QM system. The GMP-compliant qualification of equipment and systems as well as validation to demonstrate the reproducibility of manufacturing processes, cleaning methods, analytical methods and computerized systems is based on a risk-based approach. The criticality determines the depth of the respective test efforts.
Valicare GmbH offers the customers all commercially available services in this area at the highest professional and technical level.
Risk management according to EN ISO 14971 represents an essential part of quality assurance in the medical device manufacturing industry. The implementation and systematic application of the norm specifications enables the companies to eliminate or minimize the risks of their medical devices through conceptual or constructive measures.
Valicare GmbH offers the following services for this purpose:
Benefit from our long-term experience and expertise in the field of risk management.