Creation of design history files for medical devices
Testo Industrial Services took over the creation of Design History Files according to DIN EN ISO 13485 for medical devices for the company Sunstar Deutschland GmbH. Concept development, risk analyses, GAP analyses and technical documentation were also part of the service.
Sunstar, founded in 1932, is an international Japanese company with more than 4,000 employees in over 20 countries worldwide. Sunstar offers a broad product portfolio in various product categories, such as medical devices, cosmetics, consumer goods, food and nutritional supplements, and pharmaceuticals. Medical devices developed by Sunstar GUM® for use in preventive dentistry are subject to the requirements of the Medical Devices Act and must comply with the applicable European standards.
Testo Industrial Services was commissioned with the preparation of the Design History Files according to DIN EN ISO 13485 for three medical devices from the GUM® AftaClear® group. The retrospective creation of the DHF was intended to ensure that the documentation for GUM® AftaClear® products is adapted to the requirements of DIN EN ISO 13485:2016 and that the requirements for existing products are thus also met in full. As part of this, the existing documentation was checked to ensure it was up to date, together with its completeness and consistency.
I am extremely satisfied with the performance of Testo Industrial Services. During the planning phase, a sustainable strategy for the retrospective documentation of the Design History Files was created. The employees of Testo Industrial Services were highly adaptable, actively made suggestions for documentation, were flexible and solution oriented. This saved us a considerable amount of time, and internal employees were able to push ahead with other projects in parallel. The joint project was completed swiftly and successfully.
Dr. Alexander Huwig
Director Global Research and Development
Oral Care Business Unit
Sunstar Deutschland GmbH
Your advantage: Our competence
- Conceptual design phase for the creation of DHFs: Review of tech files and risk analyses, definition of approach and milestones, preparation of schedule
- Review of the existing risk analyses for the corresponding products for up-to-dateness, completeness and consistency as well as adjustment of the risk analyses
- Perform gap analysis and review tech files for discrepancies and make necessary updates and adjustments
- Summary of relevant information from the technical documentation in categories (Design Input, Design Output, Design Verification, Design Validation, User Need, Design Transfer)
- Creation of three design history files for the GUM® AftaClear® product family
Qualification
GMP-compliant qualification of cleanrooms, facilities & utilities, transport & storage
On-site calibration
Overcoming distances and reducing downtimes
Service portfolio
Your partner for calibration, test equipment management, qualification and validation