Discover how our innovative solutions can elevate your quality management to the next level.
We are motivated, flexible and creative and will support you with whatever task may have come your way! Not only will we be aiding you in finding solutions to your problems and concerns, but also supporting the concrete implementation of the necessary documentation and trainings to ensure long-lasting stability of the effects of our work. Since the company’s founding in 2009, our motivated team will bring you the fresh ideas and modern solutions you are looking for to ensure conformity not just today, but tomorrow. Using our experience working with companies all over the medical devices/pharmaceuticals industry and in contact with our wide-ranging international network of colleagues, no problem will be left unsolved!
Topics:
QMS ISO 13485, Risk Management , Lean QMS, Technical Writing, ISO 9001, MDD/MDR transition, Medical Device Regulation, Technical Documentation, Document Management, Validation, Post-Market-Surveillance, Medical Devices, Audit Remediation, Audit Preparation, Trainings, MDSAP und hands-on support
