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Not only your customers, but you, too, should feel good! We are happy to be of service - ranging from "ambulatory" to "intensive" support -

at +49 (0) 8106-92928-0

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Cross-section desired

Very few technical fields are subject to as many regulations as the production of medicines and pharmaceutical substances. There could be more regulations for Good Manufacturing Practices (GMP) than guidelines for their implementation.

The development of medical products requires the transparent and consistent documentation of each individual step from the very start. Therefore, GMP-compliant production and validation as well as development and optimisation of processes play a prominent role if scientific engineering principles and rules are used in pharmaceutical and biological technology.

Thus, our developers focus in particular on

• the definition of a consistent systematics, a project architecture and a software lifecycle,
• the creation of performance and functional specifications in accordance with approval requirements
• and the use of digital versioning and documentation software (SVN).

This is how we ensure that our customers

• remain flexible thanks to scalable project organisation,
• experience the greatest possible transparency within the project,
• can separate information into that which is approval-specific and device-specific,
• receive standardised documents directly during product development,
• can track or restore any project status at any time.

Get ahead!
Thanks to interdisciplinary co-operation during complex product developments and the implementation of your requirements in innovative product solutions.