To ensure flawless quality, the medical technology sector is subject to strict international standards. The requirements for quality management have risen sharply in the past three years, and gained considerably in complexity. This is partly due to the new Medical Device Regulation (MDR) that became effective in 2017 and becomes applicable from May 2020 onwards. This regulation contains extensive new requirements and puts a high strain on smaller companies within the medical sector in particular. In addition, DIN EN ISO 13485 is applicable to medical technology; DANmed has been certified in accordance with this standard since 2004. It includes requirements for a comprehensive management system related to the manufacture and design of medical products and is a prerequisite for approval as a manufacturer on key markets.
When a revision of the standard was announced in 2016, DANmed took the opportunity to completely realign its quality management. Until then, the company had handled its quality management using Majesty, an ERP program developed specifically for the medical technology sector, as well as Excel. However, DANmed increasingly found that the company reached its limits using this solution. To be able to guarantee the quality of its manufactured products in future, the company needed a CAQ system that could help them retrieve and evaluate production data efficiently, among other tasks, and that could also monitor incoming goods, for example.
DANmed first became aware of the BabtecQ quality management software on the ERP provider’s website. The company then took part in one of Babtec’s Q.Events, where DANmed obtained further information, had the opportunity to ask questions and talked in depth with other users and experts. The software made a good first impression and, after comparing several providers, DANmed ultimately selected the CAQ expert with a branch in nearby Villingen-Schwennigen. To provide the best possible support for its quality planning, assurance and management tasks, DANmed chose to introduce an extensive module package from the BabtecQ range.
This decision was mainly based on the scope of service and the convincing user friendliness and was further influenced by the fact that the cooperation was professional from the start. However, what ultimatleyl won DANmed over was the package offer, which allowed the company to realize quality-related tasks using software from a single source: The company was happy with several modules from day one, among them the “Gage Management”, “Task and Action Management”, “Complaints Management” and “CAPA” modules. The individual modules each met DANmed’s expectations, and so did the level of interconnectivity and consistency of data across all tasks. The latter especially made it easy to gradually introduce employees to the new system, as the intuitive design and functions of the various modules go hand in hand.
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