When the schedule is tight, an efficient process is essential. We support you with a structured and professional implementation of your CQV activities, so that the project stays on track without compromising quality or compliance.
We offer comprehensive support for the implementation and optimization of new and existing equipment. Our assistance covers the entire process – from support to the design phase and FAT activities, to installation on site, as well as commissioning and carrying out various qualification activities. In addition, we are happy to take care of the development of processes, including Cycle Development and the subsequent initial validation.
We also assist with the design of various requirements documents such as URS and CARA, etc., as well as the implementation of quality risk analyses. Through a systematic approach, we ensure that the documentation is tailored to your specific needs and complies with applicable standards and regulatory requirements.

Grundlægger af Danval ApS og freelance pharma-konsulent

Founder of Danval ApS and freelance pharma consultant